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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

7,366 ended recalls · showing 2,901 to 2,920

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  1. ENDEDClass I · Most seriousRecalled Sep 5, 2018

    Pizza Turnover, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603

    Products failed to declare allergens: Wheat and Soy

    Elaboraciones Felo, Inc. · Aguadilla, PR

    Where it was sold: Domestic distribution only (PR).

    Show details
    Product, as FDA describes it
    Pizza Turnover, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603
    Reason, in FDA's words
    Products failed to declare allergens: Wheat and Soy
    Codes on the package
    Cases are ink-stamped with production Month, Day and Shift (AM or PM).
    Where it was sold
    Domestic distribution only (PR).
    Amount recalled
    7,011 cases / 20 pieces ea
    Status
    Ended Apr 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0658-2019
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Sep 5, 2018

    Super Pizza Turnover, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603

    Products failed to declare allergens: Soy and Sulfites

    Elaboraciones Felo, Inc. · Aguadilla, PR

    Where it was sold: Domestic distribution only (PR).

    Show details
    Product, as FDA describes it
    Super Pizza Turnover, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603
    Reason, in FDA's words
    Products failed to declare allergens: Soy and Sulfites
    Codes on the package
    Cases are ink-stamped with production Month, Day and Shift (AM or PM).
    Where it was sold
    Domestic distribution only (PR).
    Amount recalled
    29,133 cases / 20 pieces ea.
    Status
    Ended Apr 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0659-2019
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Sep 5, 2018

    White Round Shell for Turnovers, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603

    Products failed to declare allergens: Wheat and Soy

    Elaboraciones Felo, Inc. · Aguadilla, PR

    Where it was sold: Domestic distribution only (PR).

    Show details
    Product, as FDA describes it
    White Round Shell for Turnovers, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603
    Reason, in FDA's words
    Products failed to declare allergens: Wheat and Soy
    Codes on the package
    Cases are ink-stamped with production Month, Day and Shift (AM or PM).
    Where it was sold
    Domestic distribution only (PR).
    Amount recalled
    52 cases / 25 pieces ea.
    Status
    Ended Apr 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0660-2019
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Sep 5, 2018

    Square Shell for Turnovers, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603

    Products failed to declare allergens: Wheat, Soy, and Red No. 40

    Elaboraciones Felo, Inc. · Aguadilla, PR

    Where it was sold: Domestic distribution only (PR).

    Show details
    Product, as FDA describes it
    Square Shell for Turnovers, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603
    Reason, in FDA's words
    Products failed to declare allergens: Wheat, Soy, and Red No. 40
    Codes on the package
    Cases are ink-stamped with production Month, Day and Shift (AM or PM).
    Where it was sold
    Domestic distribution only (PR).
    Amount recalled
    76 cases / 25 pieces ea.
    Status
    Ended Apr 30, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0661-2019
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Sep 4, 2018

    Fish Balls, packaged in a red and white plastic bag with gold font, NET WT: 14OZ (400g), UPC: 6 9530...

    Product contains undeclared allergens egg and crustacean.

    H & C Food Inc. · Brooklyn, NY

    Where it was sold: NY

    UPC 6953006450093
    Show details
    Product, as FDA describes it
    Fish Balls, packaged in a red and white plastic bag with gold font, NET WT: 14OZ (400g), UPC: 6 953006 4 50093. Keep Frozen.
    Reason, in FDA's words
    Product contains undeclared allergens egg and crustacean.
    Codes on the package
    Product is not coded.
    Where it was sold
    NY
    Amount recalled
    Unknown
    Status
    Ended Nov 14, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0003-2019
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Sep 4, 2018

    Fuzhou Fish Balls, packaged in a blue and white package bag, in two sizes: Net WT: 14 OZ (400g), U...

    Product contains undeclared allergens, egg, crustacean, and pork.

    H & C Food Inc. · Brooklyn, NY

    Where it was sold: NY

    UPC 6953640050017
    Show details
    Product, as FDA describes it
    Fuzhou Fish Balls, packaged in a blue and white package bag, in two sizes: Net WT: 14 OZ (400g), UPC: 6 953640 05000 and Net WT:4.5 lbs. (2043g), UPC: 6 953640 050017. Keep Frozen.
    Reason, in FDA's words
    Product contains undeclared allergens, egg, crustacean, and pork.
    Codes on the package
    Product is not coded.
    Where it was sold
    NY
    Amount recalled
    N/A
    Status
    Ended Nov 14, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0004-2019
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Aug 29, 2018

    CedarLane Organic Salads; Couscous, Veggies & Chickpeas with Citrus Dressing. NET WT 9 oz. -Glu...

    Discovery that the product is labeled as gluten free but contains wheat (couscous). Wheat is not declared as an allergen

    Cedarlane Natural Foods Inc/Frankly Fresh Foods Inc. · Carson, CA

    Where it was sold: One grocery chain - sent to DC's in FL. CO. PA, IN, IL, TX, OR, CA, GA.

    UPC 038794999040
    Show details
    Product, as FDA describes it
    CedarLane Organic Salads; Couscous, Veggies & Chickpeas with Citrus Dressing. NET WT 9 oz. -Gluten Free -Vegetarian Perishable, Keep Refrigerated. UPC: 38794 99904 Manufactured and Distributed by: CedarLane Foods, Carson, CA 90746
    Reason, in FDA's words
    Discovery that the product is labeled as gluten free but contains wheat (couscous). Wheat is not declared as an allergen
    Codes on the package
    Expiration dates of 9/05/2018 to 10-19-2018
    Where it was sold
    One grocery chain - sent to DC's in FL. CO. PA, IN, IL, TX, OR, CA, GA.
    Amount recalled
    579 cases (8 x 9 oz. containers per case)
    Status
    Ended Oct 10, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1969-2018
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Aug 20, 2018

    Mexican Style Ricotta Cheese labeled, "Don Froylan Requeson***Mexican Style Ricotta Cheese***Ingredi...

    Don Froylan Requeson is being recalled because the ingredient statement does not declare milk, a major food allergen. The pasteurized whey comes from ...

    Ochoa's Queseria LLC · Albany, OR

    Where it was sold: Firm distributes to wholesale accounts, retailers, and restaurants in Oregon and Washington

    Show details
    Product, as FDA describes it
    Mexican Style Ricotta Cheese labeled, "Don Froylan Requeson***Mexican Style Ricotta Cheese***Ingredients: Pasteurized Whey, Salt***" 1lb. (16 oz.) and bulk plastic bags in 2lb. and 5lb.
    Reason, in FDA's words
    Don Froylan Requeson is being recalled because the ingredient statement does not declare milk, a major food allergen. The pasteurized whey comes from whole milk.
    Codes on the package
    Use By Dates: 8/22/2018, 8/23/2018, 8/24/2018, 8/25/2018, 8/29/2018, 8/30/2018, 8/31/2018, 9/01/2018, 9/05/2018, 9/06/2018, 9/07/2018, 9/08/2018, 9/12/2018, 9/13/2018, 9/14/2018, 8/15/2018
    Where it was sold
    Firm distributes to wholesale accounts, retailers, and restaurants in Oregon and Washington
    Amount recalled
    1357 total units (1330 units of 1 lb.; 3 bags of 5lb (15 units); 6 bags of 2lb (12 units))
    Status
    Ended Sep 18, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1908-2018
    View in FDA's recall database
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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

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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.

At the store?

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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.