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FDA FOOD RECALLS

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Every FDA food recall since 2012, in one place. We check each recall's status with FDA every day.

Checked with FDA daily · Source: U.S. Food and Drug Administration

7,651 recalls · showing 3,181 to 3,200

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  1. ENDEDClass II · ModerateRecalled Aug 17, 2018

    Tipu's Chai - Sweetened Masala Chai, Net wt.7.5 oz. per box. UPC #: 7 19196 20035 3. Each box conta...

    Product is recalled due to undeclared milk. Sweetened Masala Chai boxes contain five single serve sachet packets of Chai Tea Latte, which declares mi...

    Tipu'S Chai · Polson, MT

    Where it was sold: Distributed in CA

    UPC 719196200353UPC 719196200735
    Show details
    Product, as FDA describes it
    Tipu's Chai - Sweetened Masala Chai, Net wt.7.5 oz. per box. UPC #: 7 19196 20035 3. Each box contains five single serve sachet packets of Chai Tea Latte. Single serve sachet Chai Tea Latte packets, net wt. 1.1 oz per packet. UPC 7 19196 20073 5. The LABEL of Sweetened Masala Chai is read in parts: "***SWEETENED MASALA CHAI add water + milk ***NET WT. 7.5 OZ ***INGREDIENTS: Organic dry cane syrup, black tea, organic spices. The LABEL of single serve sachet Chai Tea Latte packet is read in part "***CHAI TEA LATTE simply add water *** NETWT 1.1 OZ ***INGREDIENTS: Organic dry cane syrup, Milk powder (Concentrated nonfat milk, cream, lactose, sunflower lecithin, Vitamin A palmitate and Vitamin D3, Tocopherols (a natural source of Vitamin E to protect flavor)), Instantized black tea, Organice spices, Ginger.
    Reason, in FDA's words
    Product is recalled due to undeclared milk. Sweetened Masala Chai boxes contain five single serve sachet packets of Chai Tea Latte, which declares milk, but Sweetened Masala Chai boxes do not declare milk.
    Codes on the package
    Lot Code on 7.5 oz. BOXES: 18093 Enjoy By Date on 7.5 oz. BOXES: 10/3/19
    Where it was sold
    Distributed in CA
    Amount recalled
    60 Retail Box Units
    Status
    Ended Oct 12, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1857-2018
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Aug 17, 2018

    Aztlan Mole Poblano; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, peanut, s...

    During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen stat...

    Hidroponicos Brownia, S.P.R. de R.L. · Ciudad De Mexico, N/A

    Where it was sold: California

    Show details
    Product, as FDA describes it
    Aztlan Mole Poblano; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, peanut, soybean oil, pasilla pepper, guajillo pepper, sesame seed, cookie, cocoa, corn flour, idozided salt, condiments and spices. Sodium benzoate as a preservative. Distributed by/distributed for: Jelley Crown Inc. City of Industry, CA
    Reason, in FDA's words
    During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen statement
    Codes on the package
    Mole Pablano: lots 3757, 3769, 3998, 4038.
    Where it was sold
    California
    Amount recalled
    650 x 10 kg barrels
    Status
    Ended Feb 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1980-2018
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Aug 17, 2018

    Aztlan Mole Oaxaqueno Negro; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, p...

    During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen stat...

    Hidroponicos Brownia, S.P.R. de R.L. · Ciudad De Mexico, N/A

    Where it was sold: California

    Show details
    Product, as FDA describes it
    Aztlan Mole Oaxaqueno Negro; 10 kg plastic buckets (22 lbs); Ingredients: sugar, Ancho pepper, peanut, soybean oil, pasilla pepper, guajillo pepper, sesame seed, cookie, cocoa, corn flour, idozided salt, condiments and spices. Sodium benzoate as a preservative. Distributed by/distributed for: Jelley Crown Inc. City of Industry, CA
    Reason, in FDA's words
    During FDA foreign inspection of manufacturer, it was discovered that milk, wheat and soy were not declared as sub ingredients or in the allergen statement
    Codes on the package
    Mole Oaxaqueno Negro: lots 3750, 3765, 3936, 3989.
    Where it was sold
    California
    Amount recalled
    450 x 10 kg barrels
    Status
    Ended Feb 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1981-2018
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Aug 17, 2018

    Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition f...

    Undeclared almonds on the labeling

    Neighbors LLC · West Monroe, LA

    Where it was sold: Products were distributed in the following states: AL, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, MI, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, ...

    Show details
    Product, as FDA describes it
    Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients: Whole grain sorghum flour, cane sugar, semi sweet chocolates**Contains eggs, milk and soy.***Manufactured in the same equipment that manufactures peanut, walnut, pecan, macadamia nut, milk, soy, wheat, egg and almond products***
    Reason, in FDA's words
    Undeclared almonds on the labeling
    Codes on the package
    17289, 18050
    Where it was sold
    Products were distributed in the following states: AL, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, MI, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WV, & WI.
    Amount recalled
    7,264 Units
    Status
    Ended Aug 4, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1991-2018
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Aug 15, 2018

    Chocolate Chip Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each m...

    Chocolate Chip Cookies are recalled because cookies may contain undeclared peanuts.

    Marsee Foods Inc · Portland, OR

    Where it was sold: Distributed in Oregon and Washington

    Show details
    Product, as FDA describes it
    Chocolate Chip Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The label on master case is read "***Cafe YUMM! Chocolate Chip Cookies ***Perishable Keep Frozen *** 48 items *** Manufactured exclusively for Beau Delicious! International dba Caf¿ Yumm! 456 Charnelton St, Eugene, OR 97401.***" The affected cookies were sold at Caf¿ Yumm! restaurants. The cookies are prepared as both a chocolate-dipped and undipped version and are served on a plate for dine-in restaurant guests or offered in a pastry bag for take-out orders.
    Reason, in FDA's words
    Chocolate Chip Cookies are recalled because cookies may contain undeclared peanuts.
    Codes on the package
    Lot codes used on unopened cases will read 200, 201, 202, 203, or 204. The master cases has a manufacturing dates: 08 06, 08 07, 08 08, 08 09, 08 10, 08 11, 08 12, 08 13, 08 14, and 08 15. The individual cookies and the boxes (24 counts) are not labeled or affixed with dates, so once the individual cookies or the box (24 counts) removed from the master case by the restaurants the dates and labels are no longer available/track.
    Where it was sold
    Distributed in Oregon and Washington
    Amount recalled
    96 cases
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1852-2018
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Aug 15, 2018

    Ginger Spice Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each mas...

    Ginger Spice Cookies are recalled because cookies may contain undeclared peanuts.

    Marsee Foods Inc · Portland, OR

    Where it was sold: Distributed in Oregon and Washington

    Show details
    Product, as FDA describes it
    Ginger Spice Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The label on master case is read "***Cafe YUMM! Ginger Spice Cookies ***Perishable Keep Frozen *** 48 items *** Manufactured exclusively for Beau Delicious! International dba Caf¿ Yumm! 456 Charnelton St, Eugene, OR 97401.***" The affected cookies were sold at Caf¿ Yumm! restaurants. The cookies are prepared as both a chocolate-dipped and undipped version and are served on a plate for dine-in restaurant guests or offered in a pastry bag for take-out orders.
    Reason, in FDA's words
    Ginger Spice Cookies are recalled because cookies may contain undeclared peanuts.
    Codes on the package
    Lot codes used on unopened cases will read 200, 201, 202, 203, or 204. The master cases has a manufacturing dates: 08 06, 08 07, 08 08, 08 09, 08 10, 08 11, 08 12, 08 13, 08 14, and 08 15. The individual cookies and the boxes (24 counts) are not labeled or affixed with dates, so once the individual cookies or the box (24 counts) removed from the master case by the restaurants the dates and labels are no longer available/track.
    Where it was sold
    Distributed in Oregon and Washington
    Amount recalled
    96 cases
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1853-2018
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Aug 15, 2018

    Oatmeal Raisin Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each m...

    Oatmeal Raisin Cookies are recalled because cookies may contain undeclared peanuts.

    Marsee Foods Inc · Portland, OR

    Where it was sold: Distributed in Oregon and Washington

    Show details
    Product, as FDA describes it
    Oatmeal Raisin Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The label on master case is read "***Cafe YUMM! Oatmeal Raisin Cookies ***Perishable Keep Frozen *** 48 items *** Manufactured exclusively for Beau Delicious! International dba Caf¿ Yumm! 456 Charnelton St, Eugene, OR 97401.***" The affected cookies were sold at Caf¿ Yumm! restaurants. The cookies are prepared as both a chocolate-dipped and undipped version and are served on a plate for dine-in restaurant guests or offered in a pastry bag for take-out orders.
    Reason, in FDA's words
    Oatmeal Raisin Cookies are recalled because cookies may contain undeclared peanuts.
    Codes on the package
    Lot codes used on unopened cases will read 200, 201, 202, 203, or 204. The master cases has a manufacturing dates: 08 06, 08 07, 08 08, 08 09, 08 10, 08 11, 08 12, 08 13, 08 14, and 08 15. The individual cookies and the boxes (24 counts) are not labeled or affixed with dates, so once the individual cookies or the box (24 counts) removed from the master case by the restaurants the dates and labels are no longer available/track.
    Where it was sold
    Distributed in Oregon and Washington
    Amount recalled
    48 cases
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1854-2018
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Aug 14, 2018

    Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. ...

    Chocolate Gooey Brownie Ice Cream is recalled due to possible undeclared peanuts.

    SALT & STRAW LLC · Portland, OR

    Where it was sold: Distributed in CA, OR, and WA. Firm also sold via saltandstraw.com to internet consumers and shipped to AZ, CA, CO, CT, DE, FL, GA, IA, IL, KY, LA, MA, MD, ME, MI, MN, NH, NJ, N...

    Show details
    Product, as FDA describes it
    Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3 gal. tubs. 3 gal. tubs were sold to Salt & Straw Retail Scoop Shops only. 1 gal. containers are sold to wholesale accounts only.
    Reason, in FDA's words
    Chocolate Gooey Brownie Ice Cream is recalled due to possible undeclared peanuts.
    Codes on the package
    ***For PINTS sold to consumers: 41-404 (plant code): lot numbers 18201, 18203, 18212, 18213, 18214, 18219, 18221, and 18223. 06-1626F (plant code): lot numbers 18217, 18219, and 18221. ***For 3-GAL sold to Salt & Straw retail Scoop Shops: 41-404 (plant code): Lot numbers: 180718, 180719-B, 180722, 180731, 180801, 180802, 180804, 180807, 180809, and 180811. 06-1626F (plant code): lot numbers: 180805, 180807, 180808, and 180809. ***For 1-GAL containers sold to wholesale accounts: 41-404 (plant code): lot number 18201, 18204, 18216, 18222
    Where it was sold
    Distributed in CA, OR, and WA. Firm also sold via saltandstraw.com to internet consumers and shipped to AZ, CA, CO, CT, DE, FL, GA, IA, IL, KY, LA, MA, MD, ME, MI, MN, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, and WI.
    Amount recalled
    4,088 Pints; 661/3 Gallon Tubs; 18/1 Gallon Tubs
    Status
    Ended Feb 8, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1846-2018
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Aug 9, 2018

    Chef s Request professional steak marinade and Buckhead wildlife marinade, 12oz, 64oz, 1 gallon; sh...

    Deli Star Inc. dba King's Food Products initiated a voluntary recall of Chef s Request professional steak marinade and Buckhead wildlife marinade due...

    Deli Star Ventures Inc. dba King's Food Products · Belleville, IL

    Where it was sold: Domestic: Illinois Foreign/VA/DOD: None

    Show details
    Product, as FDA describes it
    Chef s Request professional steak marinade and Buckhead wildlife marinade, 12oz, 64oz, 1 gallon; shelf stable, refrigerate after opening
    Reason, in FDA's words
    Deli Star Inc. dba King's Food Products initiated a voluntary recall of Chef s Request professional steak marinade and Buckhead wildlife marinade due to undeclared allergens soy and wheat.
    Codes on the package
    Chef s request internal item number 13255 Buckhead internal item number 13259 Production Date/Production lot Code 7-26-18 82071 2-16-18 80471 1-18-18 80181 10-2-17 72751 7-18-17 71991 7-17-17 71981 1-20-17 70201
    Where it was sold
    Domestic: Illinois Foreign/VA/DOD: None
    Amount recalled
    4,715lbs. of buckead and 4,088.5lbs of chefs request
    Status
    Ended Feb 7, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0619-2019
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Aug 8, 2018

    Tomato Condensed Soup, 26 oz (1 LB 10 OZ) 737 g, 307 x 512 Can, Family Size, 12 cans per tray, she...

    Morgan Foods, Inc. initiated a voluntary recall of Tomato Condensed Soup, 26 oz. (1 LB 10 OZ) 737 g can, due to being mislabeled and containing cream ...

    Morgan Foods, Inc. · Austin, IN

    Where it was sold: Domestic: AR Foreign/VA/DOD: None

    UPC 787420432399
    Show details
    Product, as FDA describes it
    Tomato Condensed Soup, 26 oz (1 LB 10 OZ) 737 g, 307 x 512 Can, Family Size, 12 cans per tray, shelf stable
    Reason, in FDA's words
    Morgan Foods, Inc. initiated a voluntary recall of Tomato Condensed Soup, 26 oz. (1 LB 10 OZ) 737 g can, due to being mislabeled and containing cream of mushroom soup with undeclared allergens milk and soy.
    Codes on the package
    May 29, 2018 [E2918 batch code on can]; UPC: 78742043239 [On label] 3-Digit Code: GTY [On bottom of can] Batch: E2918 [On bottom of can]
    Where it was sold
    Domestic: AR Foreign/VA/DOD: None
    Amount recalled
    6,168 cans
    Status
    Ended Apr 29, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1855-2018
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Aug 7, 2018

    Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutriti...

    Product is labeled as gluten free, however, it contains wheat.

    Graeters Manufacturing Company · Cincinnati, OH

    Where it was sold: Products were distributed in the following states: CA, FL, IL, IN, KY, MD, MI, NJ, NY, OH, PA, TX, UT, VA & WA.

    Show details
    Product, as FDA describes it
    Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN FREE**INGREDIENTS: CREAM, MILK, CANE SUGAR, GRAHAM PIE PIECES, WHEAT FLOUR**CONTAINS:MILK, EGG, WHEAT,& SOY**Manufactured by: Graeter's Ice Cream, Cincinnati, OH**
    Reason, in FDA's words
    Product is labeled as gluten free, however, it contains wheat.
    Codes on the package
    18183390186
    Where it was sold
    Products were distributed in the following states: CA, FL, IL, IN, KY, MD, MI, NJ, NY, OH, PA, TX, UT, VA & WA.
    Amount recalled
    4,056 Pints
    Status
    Ended Mar 4, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1837-2018
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Aug 6, 2018

    BulkSupplements.com Glucosamine Sulfate Potassium; 100 grams, 250 grams, 500 grams, 1 kilogram; St...

    FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on w...

    Hard Eight Nutrition LLC · Henderson, NV

    Where it was sold: Worldwide sales from website and Amazon. Foreign distribution to: " Australia " Austria " Canada " Czech Republic " Denmark " Finland " France " Germany " Iceland " Isle ...

    Show details
    Product, as FDA describes it
    BulkSupplements.com Glucosamine Sulfate Potassium; 100 grams, 250 grams, 500 grams, 1 kilogram; Stand up zipper pouch bags. Directions: As a dietary supplement, take 1000 mg (scant 1/4 tsp) up to three time daily, or as directed by a physician. Distributed exclusively by: Bulk Supplements.com 7511 Eastgate Road Henderson, NV 89011
    Reason, in FDA's words
    FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website.
    Codes on the package
    Lot: 121D1214, Exp: 12/13/18; Lot: 121E0629, Exp: 06/28/19.
    Where it was sold
    Worldwide sales from website and Amazon. Foreign distribution to: " Australia " Austria " Canada " Czech Republic " Denmark " Finland " France " Germany " Iceland " Isle of Man " Italy " Japan " Liechtenstein " Luxembourg " Netherlands " New Zealand " Norway " South Africa " Sweden " Switzerland " The Philippines " United Kingdom
    Amount recalled
    2,100 units
    Status
    Ended Dec 19, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1827-2018
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Aug 3, 2018

    FUSIA Asian Inspirations Spicy Mongolian Noodle Bowl, NET WT 8.5 OZ (240g) Heat and Serve UPC# 0414...

    Inner packaging contains undeclared peanuts.

    Marketing Concepts Group · Weston, CT

    Where it was sold: IL

    UPC 041498135461
    Show details
    Product, as FDA describes it
    FUSIA Asian Inspirations Spicy Mongolian Noodle Bowl, NET WT 8.5 OZ (240g) Heat and Serve UPC# 041498135461 PRODUCT OF CHINA
    Reason, in FDA's words
    Inner packaging contains undeclared peanuts.
    Codes on the package
    Lot Code: SH 8097 PEAN22 4
    Where it was sold
    IL
    Amount recalled
    59,333 PIECES
    Status
    Ended Sep 14, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1819-2018
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Aug 3, 2018

    Mediterranean Salad Vegan, pre-packaged. UPC 0 211004 706991.

    Mediterranean Salad Vegan is recalled because milk is declared in the Ingredients statement but it is not declared in the Contains statement.

    Market of Choice Inc · Eugene, OR

    Where it was sold: Distributed in OR.

    UPC 211004706991
    Show details
    Product, as FDA describes it
    Mediterranean Salad Vegan, pre-packaged. UPC 0 211004 706991.
    Reason, in FDA's words
    Mediterranean Salad Vegan is recalled because milk is declared in the Ingredients statement but it is not declared in the Contains statement.
    Codes on the package
    Sell by dates: 7/29/18 to 08/07/2018
    Where it was sold
    Distributed in OR.
    Amount recalled
    138 units
    Status
    Ended Aug 22, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1826-2018
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Aug 3, 2018

    Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend, Net Wt. 15 lbs (6 / 2.5 lb bags pe...

    Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend is recalled due to undeclared wheat.

    J R Simplot Co Corporate HQ · Boise, ID

    Where it was sold: distributed in CA, CO, CT, FL, GA, KS, MD, MI, MT, NC, NV, NY, PA, VA, WA, and WI.

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    Product, as FDA describes it
    Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend, Net Wt. 15 lbs (6 / 2.5 lb bags per case), UPC 1007117012948, Distributed by JR Simplot Co. PO Box 9386, Boise, ID 83707. Product is frozen. The label is read in parts: "***EXOTIC GRAINS & FIRE-ROASTED VEGETABLE BLEND ***Red & brown rice, black beans, roasted corn, red quinoa, tomato, bell pepper, roasted Anaheim & yellow bell peppers, onions, amaranth, roasted garlic & seasoning***Gluten Free***Vegan***DO NOT DROP- STORE AT 0 F OR BELOW***".
    Reason, in FDA's words
    Simplot Good Grains Exotic Grains & Fire-Roasted Vegetable Blend is recalled due to undeclared wheat.
    Codes on the package
    389 MAY 04 18 20 389 JUL 10 18 20
    Where it was sold
    distributed in CA, CO, CT, FL, GA, KS, MD, MI, MT, NC, NV, NY, PA, VA, WA, and WI.
    Amount recalled
    379 cases (6/2.5 lb. bags per case)
    Status
    Ended Sep 19, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1844-2018
    View in FDA's recall database
  16. ENDEDClass I · Most seriousRecalled Aug 1, 2018

    Blue Diamond Almond Breeze Almond Milk, Half Gallon

    HP Hood LLC, has initiated a recall of Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.

    HP Hood LLC · Winchester, VA

    Sold in the U.S. (states not listed)

    Where it was sold: Product was distributed in the continental US in 24 states.

    Show details
    Product, as FDA describes it
    Blue Diamond Almond Breeze Almond Milk, Half Gallon
    Reason, in FDA's words
    HP Hood LLC, has initiated a recall of Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.
    Codes on the package
    SEP 02 18 HH:MM (military time) H5 L# (1 or 2) 51-4109.
    Where it was sold
    Product was distributed in the continental US in 24 states.
    Amount recalled
    24,209 cases (72,627 gallons) distributed
    Status
    Ended Nov 4, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1832-2018
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Aug 1, 2018

    Sweet Earth Foods Aloha BBQ Quesadilla; 2 pack, NET WT 8 oz. Vegan: Pinto Beans, Red Onions, Pinea...

    Firm received complaints of Sweet Earth Aloha BBQ Quesadilla packages that contain Mile High Quesadillas. Ingredient statement on outer package does n...

    Sweet Earth Inc. · Moss Landing, CA

    Where it was sold: DC's in TX, CA, IL, IA, FL, MD

    UPC 016741000551
    Show details
    Product, as FDA describes it
    Sweet Earth Foods Aloha BBQ Quesadilla; 2 pack, NET WT 8 oz. Vegan: Pinto Beans, Red Onions, Pineapple and jalapenos with our vegan BBQ grounds and a cheddar-style vegan cheese. Keep Frozen. Ingredients: Filling: Vegan BBQ savory grounds (water, vital wheat gluten, onion, soy sauce, (water, soybeans, wheat, salt, alcohol), tomato paste, molasses, apple cider vinegar, canola oil, brown rice syrup, spices, nutritional yeast, garlic powder, bell pepper, ginger, natural hickory smoke, rice bran oil, rice vinegar, oregano, pinto beans (water, pinto beans), vegan cheddar style cheese (filtered water, coconut oil, modified food starch, {potato and corn], potato starch, sea salt, vegan cheddar flavor, olive oil extract, beta carotene, vitamin B12, red onion, pineapple (pineapple, pineapple juice and citric acid) Canola oil, jalapeno pepper, spices. WRAP: Water, unbleached white flour, canola oil, sea salt, baking powder (sodium bicarbonate, sodium acid pyrophosphate, potato starch) yeast, citric acid. Contains Soy, Wheat Manufactured in a facility that process egg, milk tree nuts. UPC: 016741000551 Sweet Earth Foods Moss Landing, CA 95039
    Reason, in FDA's words
    Firm received complaints of Sweet Earth Aloha BBQ Quesadilla packages that contain Mile High Quesadillas. Ingredient statement on outer package does not declare eggs or milk.
    Codes on the package
    Lot 8149; Best By Date: 6/28/2019
    Where it was sold
    DC's in TX, CA, IL, IA, FL, MD
    Amount recalled
    2453 casaes
    Status
    Ended Oct 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1834-2018
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Jul 27, 2018

    TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag,...

    Roasted Chestnut loose leaf tea contains undeclared slivered almonds.

    Teasource · Saint Paul, MN

    Where it was sold: AL, CO, FL, IA, ID, IL, IN, MI, MN, NC, ND, NY, OK, OR, SC, TX, WI

    Show details
    Product, as FDA describes it
    TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag, and 4 oz., and 2 oz. resealable foil bags. teasource.com, 2616 Cleveland Ave N, Roseville, MN 55113.
    Reason, in FDA's words
    Roasted Chestnut loose leaf tea contains undeclared slivered almonds.
    Codes on the package
    Item #4322
    Where it was sold
    AL, CO, FL, IA, ID, IL, IN, MI, MN, NC, ND, NY, OK, OR, SC, TX, WI
    Amount recalled
    52 packages total
    Status
    Ended Sep 12, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1841-2018
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Jul 27, 2018

    El Guapo Jamaica Hibiscus Flowers in flexible pouches , 1 oz., 2 oz., 8 oz., 16 oz., and 10 lb. bo...

    Mojave Foods Corporation has initiated a recall of its El Guapo Jamaica Hibiscus Flowers in flexible pouches (1 oz., 2 oz., 8 oz., 16 oz., 10 lb.) . ...

    Mojave Foods Corp. · Commerce, CA

    Where it was sold: Product shipped predominantly to the Southwestern United States with the following states receiving product: Alabama, Arizona, California, Colorado, Florida, Georgia, Idaho, Oregon...

    UPC 044989201911UPC 044989005229UPC 044989012890UPC 044989013347and 1 more in the details
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    Product, as FDA describes it
    El Guapo Jamaica Hibiscus Flowers in flexible pouches , 1 oz., 2 oz., 8 oz., 16 oz., and 10 lb. box .
    Reason, in FDA's words
    Mojave Foods Corporation has initiated a recall of its El Guapo Jamaica Hibiscus Flowers in flexible pouches (1 oz., 2 oz., 8 oz., 16 oz., 10 lb.) . UPC # 044989201911, UPC # 044989005229, UPC # 044989012890, UPC # 044989013347,UPC # 079466071985, because of undeclared allergen.
    Codes on the package
    UPC # 044989201911- BEST BY Apr/02/21, BEST BY MAY/21/21; UPC # 044989005229- BEST BY Apr/07/21, Apr/16/21, Apr/17/21, May/16/21, May/19/21; UPC # 044989012890- BEST BY Apr/15/21, Apr/16/21, May/19/21, May/20/21 , UPC # 044989013347 Date Code on the package: 8109 through 8146 , UPC # 079466071985 Date Code on the package: Packaged on 4/13/18 through Packaged on 5/14/18
    Where it was sold
    Product shipped predominantly to the Southwestern United States with the following states receiving product: Alabama, Arizona, California, Colorado, Florida, Georgia, Idaho, Oregon, New Mexico, Nevada, Tennessee, Texas, Utah
    All UPCs
    044989201911, 044989005229, 044989012890, 044989013347, 079466071985
    Amount recalled
    53081 Pouches Dist.
    Status
    Ended Nov 4, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1931-2018
    View in FDA's recall database
  20. ENDEDClass III · Low riskRecalled Jul 25, 2018

    Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expira...

    Severino Pasta Manufacturing, Inc. has initiated a recall of their Severino Pasta Super Fresh Cheese Raviolini due to undeclared eggs. The retail unit...

    Severino Pasta Manufacturing, Inc. · Westmont, NJ

    Where it was sold: Product was distributed to Whole Foods Markets in the Florida and the NE/NA Region (Massachusetts, Connecticut, Rhode Island, New Hampshire, Maine) Whole Foods Florida DC, 2700 ...

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    Product, as FDA describes it
    Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.
    Reason, in FDA's words
    Severino Pasta Manufacturing, Inc. has initiated a recall of their Severino Pasta Super Fresh Cheese Raviolini due to undeclared eggs. The retail unit has the correct label on top, Cheese Raviolini which declares the precense of eggs in the ingredient statement and contains statement. However, the product has the incorrect label on the bottom, Cheese Rigatoni, which does not declare eggs in the ingredient statement or contains statement. The Raviolini label declares: Wheat, Milk, and Eggs whereas the Rigatoni label declares: Wheat and Milk. Since both labels are on the product consumers may be confused as to which ingredients are actually present.
    Codes on the package
    Not listed
    Where it was sold
    Product was distributed to Whole Foods Markets in the Florida and the NE/NA Region (Massachusetts, Connecticut, Rhode Island, New Hampshire, Maine) Whole Foods Florida DC, 2700 NW 19th Street, Ste 100, Pompano Beach, FL. Whole Foods NE/NA DC, 400 East Johnson Ave, Cheshire, CT. 06410
    Amount recalled
    42 cases, 378 units were produced
    Status
    Ended Oct 14, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1823-2018
    View in FDA's recall database

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What the classes mean

Class I · Most serious. FDA's highest level: products that could cause serious health problems or death.

Class II · Moderate. It may cause temporary health problems, or the risk of serious harm is remote.

Class III · Low risk. Not likely to cause health problems, but it breaks a labeling or manufacturing rule.

If you have a recalled product

  1. Match the codes on your package to the recall.
  2. If they match, don't eat it.
  3. Return it to the store or throw it away, as the company directs.
  4. If you feel sick, contact your doctor.

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Recall information comes from FDA's enforcement reports through openFDA. FDA publishes new reports weekly; we check every recall's status daily. This page is for information only and is not medical advice. Meat, poultry and egg products are recalled by USDA, not FDA, and are not listed here.