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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 5,081 to 5,100

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  1. ENDEDClass I · Most seriousRecalled Mar 29, 2016

    Yogurt Super Soynuts packaged in 16 oz. plastic bags and packaged in holiday tins. Lee Seed Company,...

    Product contains undeclared milk.

    Lee Seed Co Inc · Inwood, IA

    Where it was sold: Sold via the firm's website and distributed by mail nationwide since at least November 2013 to March 2016. No government/military consignees.

    Show details
    Product, as FDA describes it
    Yogurt Super Soynuts packaged in 16 oz. plastic bags and packaged in holiday tins. Lee Seed Company, Inc., Inwood, Iowa.
    Reason, in FDA's words
    Product contains undeclared milk.
    Codes on the package
    No lot code or expiration date are on the product labels/labeling.
    Where it was sold
    Sold via the firm's website and distributed by mail nationwide since at least November 2013 to March 2016. No government/military consignees.
    Amount recalled
    N/A
    Status
    Ended Oct 12, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1426-2016
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Mar 29, 2016

    CINNAMON ROLLS WITH CREAM CHEESE ICING Quality & Value pics BY PRICE CHOPPER NET WT 12.4 OZ (351g) I...

    The firm noticed that their allergen statement says, "May Contain Milk" instead of "Contains Milk"

    English Bay Batter Inc (Toronto) US Division · Columbus, OH

    Where it was sold: Product was shipped to New York only and then redistributed by the consignee to Connecticut, Massachusetts, Pennsylvania, Vermont, New Hampshire. No government accounts, no Canadia...

    UPC 041735073389
    Show details
    Product, as FDA describes it
    CINNAMON ROLLS WITH CREAM CHEESE ICING Quality & Value pics BY PRICE CHOPPER NET WT 12.4 OZ (351g) INGREDIENTS: ***CREAM CHEESE (PASTEURIZED MILK AND CREAM, CHEESE CULTURES***. CONTAINS WHEAT. MAY CONTAIN MILK, EGGS, SOY, PEANUTS AND TREE NUTS. DISTRIBUTED BY: PRICE CHOPPER, INC. SCHENECTADY, NY 12306 UPC 0 41735 07338 9.
    Reason, in FDA's words
    The firm noticed that their allergen statement says, "May Contain Milk" instead of "Contains Milk"
    Codes on the package
    Best by: June 07,2016, June 20, 2016, and June 28, 2016
    Where it was sold
    Product was shipped to New York only and then redistributed by the consignee to Connecticut, Massachusetts, Pennsylvania, Vermont, New Hampshire. No government accounts, no Canadian or Mexican accounts and no other foreign accounts.
    Amount recalled
    414 cs/12/12.4 oz canisters
    Status
    Ended Dec 2, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1968-2016
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Mar 28, 2016

    Meijer Plain Knot Rolls, 8 ct., Net Wt. 10 oz.; 12/case, 9.4 lbs/case

    R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. be...

    R.W. Bakers Co. Inc. · Norton Shores, MI

    Where it was sold: Domestic: MI, OH, WI, KY, IN, IL Foreign: None; VA/DOD: None

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    Product, as FDA describes it
    Meijer Plain Knot Rolls, 8 ct., Net Wt. 10 oz.; 12/case, 9.4 lbs/case
    Reason, in FDA's words
    R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. because they may contain trace amounts of undeclared peanuts.
    Codes on the package
    The lot number on the master case 16061 with a production date of 3/1/16. Product number 2035; the UPC code is 0-41250-09971-0 and is located at the bottom of the package label underneath the bar code
    Where it was sold
    Domestic: MI, OH, WI, KY, IN, IL Foreign: None; VA/DOD: None
    Amount recalled
    370 cases
    Status
    Ended Feb 10, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1306-2016
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Mar 28, 2016

    Assorted Dinner Rolls, 128 ct., Net Wt. 10.2 lbs; 16/ 8 ct./case

    R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. beca...

    R.W. Bakers Co. Inc. · Norton Shores, MI

    Where it was sold: Domestic: MI, OH, WI, KY, IN, IL Foreign: None; VA/DOD: None

    Show details
    Product, as FDA describes it
    Assorted Dinner Rolls, 128 ct., Net Wt. 10.2 lbs; 16/ 8 ct./case
    Reason, in FDA's words
    R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. because they may contain trace amounts of undeclared peanuts.
    Codes on the package
    The lot number is 16041 with a production date of 2/10/16; Product number 4180. This information is found on the master case of the product. This product does not have a UPC number
    Where it was sold
    Domestic: MI, OH, WI, KY, IN, IL Foreign: None; VA/DOD: None
    Amount recalled
    47 cases
    Status
    Ended Feb 10, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1307-2016
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Mar 28, 2016

    NuGo Slim Crunchy Peanut Butter Protein Bar, 5g net carbs, A gluten-free, soy protein bar with overa...

    Undeclared milk allergen. Brownie Bar packaged in Crunchy Peanut Butter Bar wrapper which does not list milk as an allergen under allergen informatio...

    NuGo Nutrition HQ · Oakmont, PA

    Where it was sold: Product was distributed throughout the United States. There were no international distribution.

    Show details
    Product, as FDA describes it
    NuGo Slim Crunchy Peanut Butter Protein Bar, 5g net carbs, A gluten-free, soy protein bar with overall peanut butter and chocolate taste covered in dark chocolate, Best Buy 07/28/2017, manufactured for: NuGo Nutrition 520 second Street, Oakmont, PA 15139 INGREDIENTS: SLIM PROTEIN [NON-GMO SOY CRISP (NON-GMO SOY PROTEIN, TAPIOCA, CALCIUM CARBONATE), NON-GMO SOY PROTEIN, NON-GMO RICE PROTEIN], BITTERSWEET DARK CHOCOLATE (CHOCOLATE LIQUOR, CANE SUGAR, COCOA BUTTER, VANILLA), CHICORY ROOT, VEGETABLE GLYCERINE, PEANUTS, CHOCOLATE LIQUOR, PEANUT FLOUR, ALMONDS, PEANUT EXTRACT, RICE BRAN, NATURAL FLAVORS, MICROCRYSTALLINE CELLULOSE, AND SALT. ALLERGEN INFORMATION: CONTAINS PEANUTS, ALMONDS AND SOY. MANUFACTURED ON EQUIPMENT THAT ALSO PROCESSES PRODUCTS CONTAINING TREE NUTS, MILK AND EGG. PRODUCT IS CERTIFIED PAREVE.
    Reason, in FDA's words
    Undeclared milk allergen. Brownie Bar packaged in Crunchy Peanut Butter Bar wrapper which does not list milk as an allergen under allergen information section of the ingredient statement.
    Codes on the package
    Lot # B16119A Best By: 28 JUL 17
    Where it was sold
    Product was distributed throughout the United States. There were no international distribution.
    Amount recalled
    1165 cases
    Status
    Ended Sep 14, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2094-2017
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Mar 25, 2016

    Trader Joe's Chocolate Orange Sticks, Net Wt. 18 oz (1lb 2oz) 510g, 36 units per case, UPC 00847162

    Trader Joe's Co. is recalling all codes of Trader Joe's Chocolate Orange Sticks and Trader Joe's Chocolate Raspberry Sticks because the products ma...

    Trader Joes Company · Monrovia, CA

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    Trader Joe's Chocolate Orange Sticks, Net Wt. 18 oz (1lb 2oz) 510g, 36 units per case, UPC 00847162
    Reason, in FDA's words
    Trader Joe's Co. is recalling all codes of Trader Joe's Chocolate Orange Sticks and Trader Joe's Chocolate Raspberry Sticks because the products may contain more than the stated traces of milk on the label.
    Codes on the package
    all lot codes
    Where it was sold
    US
    Amount recalled
    8115 cases
    Status
    Ended Nov 4, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0312-2017
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Mar 25, 2016

    Trader Joe's Chocolate Raspberry Sticks, Net Wt. 18 oz (1lb 2oz) 510g, 36 units per case, UPC 008471...

    Trader Joe's Co. is recalling all codes of Trader Joe's Chocolate Orange Sticks and Trader Joe's Chocolate Raspberry Sticks because the products may c...

    Trader Joes Company · Monrovia, CA

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

    Where it was sold: US

    Show details
    Product, as FDA describes it
    Trader Joe's Chocolate Raspberry Sticks, Net Wt. 18 oz (1lb 2oz) 510g, 36 units per case, UPC 00847122
    Reason, in FDA's words
    Trader Joe's Co. is recalling all codes of Trader Joe's Chocolate Orange Sticks and Trader Joe's Chocolate Raspberry Sticks because the products may contain more than the stated traces of milk on the label.
    Codes on the package
    all lot codes
    Where it was sold
    US
    Amount recalled
    6181 cases
    Status
    Ended Nov 4, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0313-2017
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Mar 25, 2016

    Fresh Food Market Cranberry Chicken Salad, UPC 207063-4XXXX, various package sizes. Product sold bo...

    Fresh Food Market Cranberry Chicken Salad is recalled because product may be mislabeled and may contain undeclared pecans, wheat, and soy.

    The Kroger Co · Cincinnati, OH

    Where it was sold: distributed in Oregon and Washington

    Show details
    Product, as FDA describes it
    Fresh Food Market Cranberry Chicken Salad, UPC 207063-4XXXX, various package sizes. Product sold both from bulk service case and self-service case random weight in deli cups. Product is privately labeled and the address is shown as QFC, 10116 NE 8th, Bellevue, WA 98004.
    Reason, in FDA's words
    Fresh Food Market Cranberry Chicken Salad is recalled because product may be mislabeled and may contain undeclared pecans, wheat, and soy.
    Codes on the package
    Sell by March 28, 2016 and Before
    Where it was sold
    distributed in Oregon and Washington
    Amount recalled
    810 lbs.
    Status
    Ended Mar 29, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2386-2016
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Mar 18, 2016

    Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle...

    Undeclared soy lecithin in 5 dietary supplements.

    NOW Foods · Bloomingdale, IL

    Where it was sold: Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR,...

    Show details
    Product, as FDA describes it
    Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and white lettering.
    Reason, in FDA's words
    Undeclared soy lecithin in 5 dietary supplements.
    Codes on the package
    Lot# 1966914, Batch# 582660
    Where it was sold
    Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY and PR. The one foreign consignee is Natulab in Japan.
    Amount recalled
    8 bottles
    Status
    Ended Jul 21, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1129-2016
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Mar 18, 2016

    Elderberry 500 mg packaged in a white and orange bottle containing 60 capsules. The bottle has a blu...

    Undeclared soy lecithin in 5 dietary supplements.

    NOW Foods · Bloomingdale, IL

    Where it was sold: Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR,...

    Show details
    Product, as FDA describes it
    Elderberry 500 mg packaged in a white and orange bottle containing 60 capsules. The bottle has a blue cap and white lettering.
    Reason, in FDA's words
    Undeclared soy lecithin in 5 dietary supplements.
    Codes on the package
    Lot# 1966914, Batch# 582660
    Where it was sold
    Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY and PR. The one foreign consignee is Natulab in Japan.
    Amount recalled
    57 bottles
    Status
    Ended Jul 21, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1130-2016
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Mar 18, 2016

    Gingko Biloba 60mg packaged in a white and orange bottle containing 120 capsules. The bottle has a ...

    Undeclared soy lecithin in 5 dietary supplements.

    NOW Foods · Bloomingdale, IL

    Where it was sold: Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR,...

    Show details
    Product, as FDA describes it
    Gingko Biloba 60mg packaged in a white and orange bottle containing 120 capsules. The bottle has a blue cap and white lettering.
    Reason, in FDA's words
    Undeclared soy lecithin in 5 dietary supplements.
    Codes on the package
    Lot# 1969778, Batch# 582552
    Where it was sold
    Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY and PR. The one foreign consignee is Natulab in Japan.
    Amount recalled
    2 bottles
    Status
    Ended Jul 21, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1131-2016
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Mar 18, 2016

    Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle ha...

    Undeclared soy lecithin in 5 dietary supplements.

    NOW Foods · Bloomingdale, IL

    Where it was sold: Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR,...

    Show details
    Product, as FDA describes it
    Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle has a blue cap and white lettering.
    Reason, in FDA's words
    Undeclared soy lecithin in 5 dietary supplements.
    Codes on the package
    Lot# 1961645, Batch# 579391
    Where it was sold
    Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY and PR. The one foreign consignee is Natulab in Japan.
    Amount recalled
    12 bottles
    Status
    Ended Jul 21, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1132-2016
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Mar 18, 2016

    Cranberry extract packaged in a white and orange bottle containing 90 capsules. The bottle has a blu...

    Undeclared soy lecithin in 5 dietary supplements.

    NOW Foods · Bloomingdale, IL

    Where it was sold: Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR,...

    Show details
    Product, as FDA describes it
    Cranberry extract packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and white lettering.
    Reason, in FDA's words
    Undeclared soy lecithin in 5 dietary supplements.
    Codes on the package
    Lot# 1961645, Batch# 579391
    Where it was sold
    Distributed to 499 consignees in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, VT, WA, WI, WV, WY and PR. The one foreign consignee is Natulab in Japan.
    Amount recalled
    3 bottles
    Status
    Ended Jul 21, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1133-2016
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Mar 17, 2016

    Thai Fusion Outpost, net weight 5.1 oz. UPC 0 99853 34255 9. Thai Fusion Bulk bag, packaged in a...

    Organic Thai Fusion Outpost 5.1 oz. packages, Organic Thai Fusion 3 lbs. bulk bags, and Organic On the Go Thai Fusion 3.4 oz cups are recalled due to...

    Paradise Farm Organics Inc · Moscow, ID

    Where it was sold: sold on AK, AL, AZ, CA, FL, GA, ID, IN, MA, MN, NJ, NY, OR, UT, and WA and in Netherland. Products were sold from www.maryjanesfarm.org.

    UPC 099853342559UPC 099853352558UPC 099853382555
    Show details
    Product, as FDA describes it
    Thai Fusion Outpost, net weight 5.1 oz. UPC 0 99853 34255 9. Thai Fusion Bulk bag, packaged in a ziploc plastic bag, net weight 3 lbs. UPC 0 99853 35255 8. Thai Fusion On the Go, packaged in microwave able paper cup with plastic lid, net wt. 3.4 oz. UPC 0 99853 38255 5.
    Reason, in FDA's words
    Organic Thai Fusion Outpost 5.1 oz. packages, Organic Thai Fusion 3 lbs. bulk bags, and Organic On the Go Thai Fusion 3.4 oz cups are recalled due to undeclared milk.
    Codes on the package
    Lot # 021091 Lot # 022492 Product was made on 02/10/16 and 02/24/16.
    Where it was sold
    sold on AK, AL, AZ, CA, FL, GA, ID, IN, MA, MN, NJ, NY, OR, UT, and WA and in Netherland. Products were sold from www.maryjanesfarm.org.
    Amount recalled
    15/5.1 oz. pouches of Outpost; 6/3.4 oz. cups of On the Go; and 12/3 lbs bags.
    Status
    Ended Aug 18, 2016 (FDA lists it as terminated)
    FDA recall number
    F-0818-2016
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Mar 17, 2016

    Label reads in part as: "Clight***Naranja*** Orange***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX**...

    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy...

    Mondelez Puerto Rico · San Juan, PR

    Where it was sold: Puerto Rico only.

    Show details
    Product, as FDA describes it
    Label reads in part as: "Clight***Naranja*** Orange***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926-7037***Made in Costa Rica"
    Reason, in FDA's words
    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy lecithin in the ingredient list and do not otherwise disclose soy as an ingredient.
    Codes on the package
    TBD
    Where it was sold
    Puerto Rico only.
    Amount recalled
    9,239 cases (total)
    Status
    Ended Jun 5, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1510-2016
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Mar 17, 2016

    Label reads in part as: "Clight***Mandarina*** Tangerine***CALORIE FREE ARTIFICIALLY FLAVORED DRINK ...

    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy...

    Mondelez Puerto Rico · San Juan, PR

    Where it was sold: Puerto Rico only.

    Show details
    Product, as FDA describes it
    Label reads in part as: "Clight***Mandarina*** Tangerine***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926-7037***Made in Costa Rica"
    Reason, in FDA's words
    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy lecithin in the ingredient list and do not otherwise disclose soy as an ingredient.
    Codes on the package
    TBD
    Where it was sold
    Puerto Rico only.
    Amount recalled
    9,239 cases (total)
    Status
    Ended Jun 5, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1511-2016
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Mar 17, 2016

    Label reads in part as: "Clight***T¿ Lim¿n*** Lemon Tea***CALORIE FREE ARTIFICIALLY FLAVORED DRINK M...

    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy...

    Mondelez Puerto Rico · San Juan, PR

    Where it was sold: Puerto Rico only.

    Show details
    Product, as FDA describes it
    Label reads in part as: "Clight***T¿ Lim¿n*** Lemon Tea***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926-7037***Made in Costa Rica"
    Reason, in FDA's words
    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy lecithin in the ingredient list and do not otherwise disclose soy as an ingredient.
    Codes on the package
    TBD
    Where it was sold
    Puerto Rico only.
    Amount recalled
    9,329 cases (total)
    Status
    Ended Jun 5, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1512-2016
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Mar 17, 2016

    Label reads in part as: "Clight***Lim¿n*** Lemon ***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***T...

    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy...

    Mondelez Puerto Rico · San Juan, PR

    Where it was sold: Puerto Rico only.

    Show details
    Product, as FDA describes it
    Label reads in part as: "Clight***Lim¿n*** Lemon ***CALORIE FREE ARTIFICIALLY FLAVORED DRINK MIX***TWO PACKAGES IN ONE***MAKES 1 LITER***NET: 0.49 oz*** Distributed by: Mondelez Puerto Rico, LLC, Montehiedra Office Center Suite 801, 9615 Ave. Los Romeros, San Juan PR 00926-7037***Made in Costa Rica"
    Reason, in FDA's words
    The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy lecithin in the ingredient list and do not otherwise disclose soy as an ingredient.
    Codes on the package
    TBD
    Where it was sold
    Puerto Rico only.
    Amount recalled
    9,239 cases (total)
    Status
    Ended Jun 5, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1513-2016
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Mar 16, 2016

    SEAFOOD BALL COMBO ASSORTI BOULETTES AUX PRODUCTS DE MER FISH BALL, FRIED FISH BALL, FRIED SHRIMP BA...

    Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.

    Way Fong LLC · Maspeth, NY

    Where it was sold: New York

    Show details
    Product, as FDA describes it
    SEAFOOD BALL COMBO ASSORTI BOULETTES AUX PRODUCTS DE MER FISH BALL, FRIED FISH BALL, FRIED SHRIMP BALL, FISH BALL WITH DACE, CUTTLEFISH BALL, Net Wt 260g/9.2oz, UPC 0 68636 05205 2, Product of Canada, KEEP REFRIGERATED
    Reason, in FDA's words
    Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.
    Codes on the package
    All lot numbers beginning with "0" and "8"
    Where it was sold
    New York
    Amount recalled
    58 cases
    Status
    Ended May 8, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1628-2016
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Mar 16, 2016

    FRIED SHRIMP FLAVOURED FISH BAR, Net Wt 9.07 Kg 4 X 5 lbs. bulk, Product of Canada, KEEP REFRIGERAT...

    Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.

    Way Fong LLC · Maspeth, NY

    Where it was sold: New York

    Show details
    Product, as FDA describes it
    FRIED SHRIMP FLAVOURED FISH BAR, Net Wt 9.07 Kg 4 X 5 lbs. bulk, Product of Canada, KEEP REFRIGERATED
    Reason, in FDA's words
    Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.
    Codes on the package
    All lot numbers beginning with "0" and "8"
    Where it was sold
    New York
    Amount recalled
    15 cases
    Status
    Ended May 8, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1629-2016
    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.