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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 ยท Source: U.S. Food and Drug Administration

7,651 recalls ยท showing 4,721 to 4,740

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  1. ENDEDClass II ยท ModerateRecalled Feb 13, 2017

    Pharmanex BioGinkgo. Mental Sharpness. 60 Tablets

    Nu Skin announces a voluntary field action for Pharmanex BioGinkgo due to undeclared allergen; wheat.

    Nu Skin Enterprises Inc. ยท Provo, UT

    Where it was sold: Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.

    Show details
    Product, as FDA describes it
    Pharmanex BioGinkgo. Mental Sharpness. 60 Tablets
    Reason, in FDA's words
    Nu Skin announces a voluntary field action for Pharmanex BioGinkgo due to undeclared allergen; wheat.
    Codes on the package
    Batches: DL14951-07, DL31551-07, DL21161-07
    Where it was sold
    Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.
    Amount recalled
    40,158
    Status
    Ended Aug 22, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1578-2017
  2. ENDEDClass II ยท ModerateRecalled Feb 13, 2017

    Pharmanex Cortitrol. Cortisol Management. 60 Capsules

    Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.

    Nu Skin Enterprises Inc. ยท Provo, UT

    Where it was sold: Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.

    Show details
    Product, as FDA describes it
    Pharmanex Cortitrol. Cortisol Management. 60 Capsules
    Reason, in FDA's words
    Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
    Codes on the package
    Batches: DL06951-08, DL14251-08, DL34351-08, DL06061-08, DL27161-08
    Where it was sold
    Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.
    Amount recalled
    56,332
    Status
    Ended Aug 22, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1579-2017
  3. ENDEDClass II ยท ModerateRecalled Feb 13, 2017

    Pharmanex Cholestin. Cholesterol Health. 60 Softgels.

    Nu Skin announces a voluntary field action for Pharmanex Cholestin due to undeclared allergen; soy.

    Nu Skin Enterprises Inc. ยท Provo, UT

    Where it was sold: Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.

    Show details
    Product, as FDA describes it
    Pharmanex Cholestin. Cholesterol Health. 60 Softgels.
    Reason, in FDA's words
    Nu Skin announces a voluntary field action for Pharmanex Cholestin due to undeclared allergen; soy.
    Codes on the package
    Batch: CS10351
    Where it was sold
    Nationwide, Canadian and other foreign consignees. No VA/govt/military consignees.
    Amount recalled
    7,327
    Status
    Ended Aug 22, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1580-2017
  4. ENDEDClass I ยท Most seriousRecalled Feb 7, 2017

    COUSINS PRODUCTS(R) Creole Tomato SALAD DRESSING, NET WT. 16 OZ (473 ML),

    One lot of Creole Tomato Salad dressing may contain Blue cheese salad dressing; undeclared milk.

    Cousins Products LLC ยท Harahan, LA

    Where it was sold: LA

    Show details
    Product, as FDA describes it
    COUSINS PRODUCTS(R) Creole Tomato SALAD DRESSING, NET WT. 16 OZ (473 ML),
    Reason, in FDA's words
    One lot of Creole Tomato Salad dressing may contain Blue cheese salad dressing; undeclared milk.
    Codes on the package
    Lot Code 0001118, Best By 05/18/17
    Where it was sold
    LA
    Amount recalled
    720 jars
    Status
    Ended May 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1622-2017
  5. ENDEDClass I ยท Most seriousRecalled Feb 6, 2017

    Fred Meyer 100% Whole Wheat Bread 16 oz plastic bag DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO ...

    During an internal investigationi at the manufacturing facility the firm discovered that hte product may contain undeclared undeclared milk.

    The Kroger Co ยท Cincinnati, OH

    Where it was sold: Product was shipped to the following states: AK, ID, OR & WA.

    UPC 011110102942
    Show details
    Product, as FDA describes it
    Fred Meyer 100% Whole Wheat Bread 16 oz plastic bag DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC 0 11110 10294 2
    Reason, in FDA's words
    During an internal investigationi at the manufacturing facility the firm discovered that hte product may contain undeclared undeclared milk.
    Codes on the package
    Julian Dates: 013 THRU 036
    Where it was sold
    Product was shipped to the following states: AK, ID, OR & WA.
    Amount recalled
    7,745/16 oz loaves
    Status
    Ended Jul 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1561-2017
  6. ENDEDClass II ยท ModerateRecalled Feb 6, 2017

    Private Selection, Salted Caramel Chocolate Almond Pie, NET WT 34 OZ ( 2 LB 2 OZ) 963g, UPC 11110540...

    Salted Carmel Chocolate Almond Pie was mislabeled. The wrong ingredient label was used which did not listed two allergens, eggs and almonds.

    Legendary Baking ยท Denver, CO

    Where it was sold: DISTRIBUTION CENTERS: OR, OH, CO, KY, AZ, WI, GA, KS. RETAIL STORES: AL, GA, SC, MI, OH, WV, IL, IN, KY, KS, MO, NE, CO, NM, UT, WY, AZ, AK, ID, OR and WA.

    UPC 011110540218
    Show details
    Product, as FDA describes it
    Private Selection, Salted Caramel Chocolate Almond Pie, NET WT 34 OZ ( 2 LB 2 OZ) 963g, UPC 1111054021. Container: In a labeled pie dome and base. Pies are distributed frozen. Some stores sell refrigerated and some sell frozen.
    Reason, in FDA's words
    Salted Carmel Chocolate Almond Pie was mislabeled. The wrong ingredient label was used which did not listed two allergens, eggs and almonds.
    Codes on the package
    lot CH 17025
    Where it was sold
    DISTRIBUTION CENTERS: OR, OH, CO, KY, AZ, WI, GA, KS. RETAIL STORES: AL, GA, SC, MI, OH, WV, IL, IN, KY, KS, MO, NE, CO, NM, UT, WY, AZ, AK, ID, OR and WA.
    Amount recalled
    652 cases
    Status
    Ended Mar 24, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1566-2017
  7. ENDEDClass II ยท ModerateRecalled Jan 30, 2017

    Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20

    Product is labeled as gluten free; however was labeled as containing an ingredient with gluten.

    Bwi Inc ยท Westlake Village, CA

    Where it was sold: U.S. distribution to the following; MA, CA, FL, UT, AZ, WI, NY, OR, IN, MO, IL, NJ, KS, CO, CT, VT, NM, HI, NV, IA, OH, WA, RI, MI. Foreign distribution to the following; Grand ...

    Show details
    Product, as FDA describes it
    Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20
    Reason, in FDA's words
    Product is labeled as gluten free; however was labeled as containing an ingredient with gluten.
    Codes on the package
    Lot #: 0217, 0317, 040617, 0517, 160603, 160711, 160810, 160921.
    Where it was sold
    U.S. distribution to the following; MA, CA, FL, UT, AZ, WI, NY, OR, IN, MO, IL, NJ, KS, CO, CT, VT, NM, HI, NV, IA, OH, WA, RI, MI. Foreign distribution to the following; Grand Cayman.
    Amount recalled
    653 cases
    Status
    Ended May 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1481-2017
  8. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Falafel King Tzatziki Sauce. 10 ounce. Plastic container

    Falafel King announced a recall for their Tzatziki Sauce due to undeclared milk on product label.

    Falafel King Ent, Inc. ยท Boulder, CO

    Where it was sold: Nationwide to Colorado, New Mexico, Utah, and Nebraska. No Canadian, other foreign, or VA/gov/military consignees.

    Show details
    Product, as FDA describes it
    Falafel King Tzatziki Sauce. 10 ounce. Plastic container
    Reason, in FDA's words
    Falafel King announced a recall for their Tzatziki Sauce due to undeclared milk on product label.
    Codes on the package
    Expiration date - 03/03/2017
    Where it was sold
    Nationwide to Colorado, New Mexico, Utah, and Nebraska. No Canadian, other foreign, or VA/gov/military consignees.
    Amount recalled
    1380 containers
    Status
    Ended May 18, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1527-2017
  9. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Goulibeur - Large pure butter shortbread with flaked almonds, in neutral gift wrapping Net weight 1...

    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the p...

    GOULIBEUR ยท Poitiers, N/A

    Where it was sold: U.S.: Maryland

    Show details
    Product, as FDA describes it
    Goulibeur - Large pure butter shortbread with flaked almonds, in neutral gift wrapping Net weight 13.5 oz
    Reason, in FDA's words
    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.
    Codes on the package
    Batch number : 16483 Best-by date : 08/15/2017
    Where it was sold
    U.S.: Maryland
    Amount recalled
    150 units
    Status
    Ended Oct 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1586-2017
  10. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Goulibeur Cube tin box with pictures of France, containing small pure butter shortbreads Net weigh...

    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the p...

    GOULIBEUR ยท Poitiers, N/A

    Where it was sold: U.S.: Maryland

    Show details
    Product, as FDA describes it
    Goulibeur Cube tin box with pictures of France, containing small pure butter shortbreads Net weight 4.23 oz
    Reason, in FDA's words
    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.
    Codes on the package
    Batch number : 16490 Best-by date : 08/15/2017
    Where it was sold
    U.S.: Maryland
    Amount recalled
    200 units
    Status
    Ended Oct 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1587-2017
  11. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Goulibeur - Pack of 15 pure butter shortbreads in 3 freshness packs Net weight 9.87 oz

    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the p...

    GOULIBEUR ยท Poitiers, N/A

    Where it was sold: U.S.: Maryland

    Show details
    Product, as FDA describes it
    Goulibeur - Pack of 15 pure butter shortbreads in 3 freshness packs Net weight 9.87 oz
    Reason, in FDA's words
    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.
    Codes on the package
    Batch number : 16490 Best-by date : 08/15/2017
    Where it was sold
    U.S.: Maryland
    Amount recalled
    240 units
    Status
    Ended Oct 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1588-2017
  12. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Goulibeur - Large French walnut shortbread, in paper carton box Net weight 9.87 oz

    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the p...

    GOULIBEUR ยท Poitiers, N/A

    Where it was sold: U.S.: Maryland

    Show details
    Product, as FDA describes it
    Goulibeur - Large French walnut shortbread, in paper carton box Net weight 9.87 oz
    Reason, in FDA's words
    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.
    Codes on the package
    Batch number : 16474 Best-by date : 08/15/2017
    Where it was sold
    U.S.: Maryland
    Amount recalled
    140 units
    Status
    Ended Oct 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1589-2017
  13. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Goulibeur- Cube tin box Life in Paris, containing mini heart-shaped pure butter shortbreads Net wei...

    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the p...

    GOULIBEUR ยท Poitiers, N/A

    Where it was sold: U.S.: Maryland

    Show details
    Product, as FDA describes it
    Goulibeur- Cube tin box Life in Paris, containing mini heart-shaped pure butter shortbreads Net weight 4.23 oz
    Reason, in FDA's words
    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.
    Codes on the package
    Batch number : 16490 Best-by date : 08/15/2017
    Where it was sold
    U.S.: Maryland
    Amount recalled
    800 units
    Status
    Ended Oct 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1590-2017
  14. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Goulibeur  2 pure butter shortbreads in a freshness bag Net weight 1.76 oz

    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the p...

    GOULIBEUR ยท Poitiers, N/A

    Where it was sold: U.S.: Maryland

    Show details
    Product, as FDA describes it
    Goulibeur  2 pure butter shortbreads in a freshness bag Net weight 1.76 oz
    Reason, in FDA's words
    This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food source for this ingredient (milk) is not indicated.
    Codes on the package
    Batch number : 16493 Best-by date : 08/15/2017
    Where it was sold
    U.S.: Maryland
    Amount recalled
    250 units
    Status
    Ended Oct 16, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1591-2017
  15. ENDEDClass III ยท Low riskRecalled Jan 27, 2017

    Assorted chocolate truffles, packaged in Kraft colored boxes with the Batch PDX sticker. Boxes cont...

    The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are declared on an insert label inside of the assorted boxes, and not declare...

    Batch International Llc ยท Beaverton, OR

    Where it was sold: distributed in AZ, CA, CO, IA, IL, MD, MI, NC, NJ, NV, NY, OR, and WA.

    Show details
    Product, as FDA describes it
    Assorted chocolate truffles, packaged in Kraft colored boxes with the Batch PDX sticker. Boxes contain 5, 8, 12, 18, 24 or 32 pieces with any combination of the following 14 flavors: 1. Vietnamese Iced Coffee 2. Raspberry 3. Spicy Passion 4. Bull Run Bourbon 5. Mint Meltaway 6. Almond Crisp 7. Yuzu Gimlet 8. Ghost Pepper 9. Almond n Coconut 10. Nutty Crunchy PDX 11. Earl Grey 12. Cinnamon 13. Dulce de Leche 14. Candy Cap Mushroom
    Reason, in FDA's words
    The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are declared on an insert label inside of the assorted boxes, and not declared on the exterior of the boxes.
    Codes on the package
    not coded
    Where it was sold
    distributed in AZ, CA, CO, IA, IL, MD, MI, NC, NJ, NV, NY, OR, and WA.
    Amount recalled
    Approximately 100-200 boxes
    Status
    Ended Mar 30, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1597-2017
  16. ENDEDClass II ยท ModerateRecalled Jan 27, 2017

    Schlabach Amish Bakery Chocolate Chip Grand-ola Bar NET WT. 2.8 OZ (80g) UPC 0 14757 13000 2 Contain...

    The was notified that their label did not list "Soy" in the ingredient statement.

    Original Amish Bakery LLC ยท Millersburg, OH

    Where it was sold: Product was sold in the following states: IL, OH & PA.

    UPC 014757130002
    Show details
    Product, as FDA describes it
    Schlabach Amish Bakery Chocolate Chip Grand-ola Bar NET WT. 2.8 OZ (80g) UPC 0 14757 13000 2 Contains: Wheat, Tree Nuts, Dairy Ingredients: Oats, chocolate chips (sugar,chocolate liquor, cocoa butter, whole milk, lecithin [an emulsifier], salt, vanilla), brown sugar, wheat, corn syrup***walnuts, soda, vanilla flavoring, cinnamon. Original Amish Bakery, LLC DBA 6007 Township road 351 Millersburg, OH 44654 P:330-674-3087
    Reason, in FDA's words
    The was notified that their label did not list "Soy" in the ingredient statement.
    Codes on the package
    Best Buy Dates: 10-10-16, 10-18-16, 10-28-16, 11-15-16, 11-16-16, 11-22-16, 12-01-16, 12-08-16, 12-20-16, 01-08-17
    Where it was sold
    Product was sold in the following states: IL, OH & PA.
    Amount recalled
    424 cases/12/2/8 oz packages + 7/2.8 oz packages
    Status
    Ended Apr 6, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1861-2017
  17. ENDEDClass I ยท Most seriousRecalled Jan 26, 2017

    Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 lbs (720g). 30 Servings. Natural V...

    Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.

    NSE Products, Inc. ยท Provo, UT

    Where it was sold: Nationwide and Canada. No other foreign or VA/govt/military consignees.

    Show details
    Product, as FDA describes it
    Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 lbs (720g). 30 Servings. Natural Vanilla Flavor. Lactose, Gluten, & Soy Free. Plant Protein/Vegetarian.
    Reason, in FDA's words
    Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
    Codes on the package
    Lot Numbers: AZ30751, AZ32051, AZ00661, AZ27161, and AZ34161
    Where it was sold
    Nationwide and Canada. No other foreign or VA/govt/military consignees.
    Amount recalled
    21,460 units
    Status
    Ended Jul 5, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1532-2017
  18. ENDEDClass II ยท ModerateRecalled Jan 26, 2017

    White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes

    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling...

    Bell Stone Toffee ยท Novi, MI

    Where it was sold: Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None

    Show details
    Product, as FDA describes it
    White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Reason, in FDA's words
    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling that declared butter as an ingredient but failed to identify the allergen milk was present in products.
    Codes on the package
    All Lots with Best By Dates Between November 18, 2016 and March 18, 2017
    Where it was sold
    Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None
    Amount recalled
    unknown
    Status
    Ended Jun 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1545-2017
  19. ENDEDClass II ยท ModerateRecalled Jan 26, 2017

    Dark Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes

    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling...

    Bell Stone Toffee ยท Novi, MI

    Where it was sold: Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None

    Show details
    Product, as FDA describes it
    Dark Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes
    Reason, in FDA's words
    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling that declared butter as an ingredient but failed to identify the allergen milk was present in products.
    Codes on the package
    All Lots with Best By Dates Between November 18, 2016 and March 18, 2017
    Where it was sold
    Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None
    Amount recalled
    unknown
    Status
    Ended Jun 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1546-2017
  20. ENDEDClass II ยท ModerateRecalled Jan 26, 2017

    Toffee Chocolate Bar, 3.5 oz

    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling...

    Bell Stone Toffee ยท Novi, MI

    Where it was sold: Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None

    Show details
    Product, as FDA describes it
    Toffee Chocolate Bar, 3.5 oz
    Reason, in FDA's words
    Bell Stone Toffee initiated a voluntary recall of all lots of White Chocolate Toffee, Dark Chocolate Toffee, and Toffee Chocolate Bars due to labeling that declared butter as an ingredient but failed to identify the allergen milk was present in products.
    Codes on the package
    All Lots with Best By Dates Between November 18, 2016 and March 18, 2017
    Where it was sold
    Domestic: MI, FL, MA, TX, GA, CO, OH Firm updated customer list to include out of state customers on 02/09/2017. Foreign:None V/A: None
    Amount recalled
    unknown
    Status
    Ended Jun 1, 2017 (FDA lists it as terminated)
    FDA recall number
    F-1547-2017

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What the classes mean

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

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

Class III ยท 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.