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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 3,701 to 3,720

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  1. ENDEDClass II · ModerateRecalled Jul 26, 2017

    Heart-Plus, No. 83, 120 Capsules, Dietary Supplement

    Undeclared allergens: soy (lecithin)

    NatureAll-STF Holding, LLC · Salt Lake City, UT

    Where it was sold: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

    Show details
    Product, as FDA describes it
    Heart-Plus, No. 83, 120 Capsules, Dietary Supplement
    Reason, in FDA's words
    Undeclared allergens: soy (lecithin)
    Codes on the package
    Lot 40800915 & 44300217
    Where it was sold
    Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
    Amount recalled
    598 bottles.
    Status
    Ended Oct 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3370-2017
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Jul 26, 2017

    Liver-Plus, No. 111 & 115, 120 Capsules, Dietary Supplement

    Undeclared allergens: soy (lecithin)

    NatureAll-STF Holding, LLC · Salt Lake City, UT

    Where it was sold: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

    Show details
    Product, as FDA describes it
    Liver-Plus, No. 111 & 115, 120 Capsules, Dietary Supplement
    Reason, in FDA's words
    Undeclared allergens: soy (lecithin)
    Codes on the package
    Lot 43000816 & 45000417
    Where it was sold
    Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
    Amount recalled
    400 bottles.
    Status
    Ended Oct 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3371-2017
    View in FDA's recall database
  3. ENDEDClass II · ModerateRecalled Jul 26, 2017

    Pancreas-Plus, No. 112, 90 Capsules, Dietary Supplement

    Undeclared allergens: soy (lecithin)

    NatureAll-STF Holding, LLC · Salt Lake City, UT

    Where it was sold: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

    Show details
    Product, as FDA describes it
    Pancreas-Plus, No. 112, 90 Capsules, Dietary Supplement
    Reason, in FDA's words
    Undeclared allergens: soy (lecithin)
    Codes on the package
    Lot 42100516 & 45400517
    Where it was sold
    Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
    Amount recalled
    566 bottles.
    Status
    Ended Oct 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3372-2017
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Jul 26, 2017

    Prostate-Plus, No. 117, 90 Capsules, Dietary Supplement

    Undeclared allergens: soy (lecithin)

    NatureAll-STF Holding, LLC · Salt Lake City, UT

    Where it was sold: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

    Show details
    Product, as FDA describes it
    Prostate-Plus, No. 117, 90 Capsules, Dietary Supplement
    Reason, in FDA's words
    Undeclared allergens: soy (lecithin)
    Codes on the package
    Lot 42700616
    Where it was sold
    Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
    Amount recalled
    186 bottles.
    Status
    Ended Oct 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3373-2017
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Jul 26, 2017

    Leci-thin-Plus, No. 88, 90 Capsules, Dietary Supplement

    Undeclared allergens: soy (lecithin)

    NatureAll-STF Holding, LLC · Salt Lake City, UT

    Where it was sold: Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

    Show details
    Product, as FDA describes it
    Leci-thin-Plus, No. 88, 90 Capsules, Dietary Supplement
    Reason, in FDA's words
    Undeclared allergens: soy (lecithin)
    Codes on the package
    Lot 41400116
    Where it was sold
    Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.
    Amount recalled
    80 bottles.
    Status
    Ended Oct 17, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3374-2017
    View in FDA's recall database
  6. ENDEDClass II · ModerateRecalled Jul 25, 2017

    CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MED...

    Missing ingredient statement on the label and undeclared soy.

    Gold Medal Products Co · Cincinnati, OH

    Where it was sold: Product was shipped to the following states: AL, AZ, CA, FL, IL, IN, MN, NC, NJ, NY, OH, OR, PA, SC, TN, TX, UT & WI. Product was also shipped to Canada.

    Show details
    Product, as FDA describes it
    CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
    Reason, in FDA's words
    Missing ingredient statement on the label and undeclared soy.
    Codes on the package
    Item #2094, Lot: 17070517004, 17070617005, 17070717006, & 17071017007
    Where it was sold
    Product was shipped to the following states: AL, AZ, CA, FL, IL, IN, MN, NC, NJ, NY, OH, OR, PA, SC, TN, TX, UT & WI. Product was also shipped to Canada.
    Amount recalled
    806 cs/12/22 oz bags
    Status
    Ended Feb 1, 2019 (FDA lists it as terminated)
    FDA recall number
    F-3469-2017
    View in FDA's recall database
  7. ENDEDClass II · ModerateRecalled Jul 22, 2017

    Hy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908996, Net Wt. 26 oz (1 lb 10 oz) 1.62 lb ...

    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list

    D & D Foods, Inc. · Omaha, NE

    Where it was sold: The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.

    UPC 288900908996
    Show details
    Product, as FDA describes it
    Hy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908996, Net Wt. 26 oz (1 lb 10 oz) 1.62 lb (737 g), West Des Moines, IA
    Reason, in FDA's words
    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
    Codes on the package
    Best if Used by Dates: 04-23-2017 thru 07-26-2017
    Where it was sold
    The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
    Amount recalled
    471/4 pizzas/cases
    Status
    Ended Sep 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3389-2017
    View in FDA's recall database
  8. ENDEDClass II · ModerateRecalled Jul 22, 2017

    Hy-Vee, Cheese Pizza, 16'' Traditional Crust, UPC 288928 611991, Net Wt. 47 oz (2 lb 15 oz) 2.94 lb ...

    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list

    D & D Foods, Inc. · Omaha, NE

    Where it was sold: The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.

    UPC 288928611991
    Show details
    Product, as FDA describes it
    Hy-Vee, Cheese Pizza, 16'' Traditional Crust, UPC 288928 611991, Net Wt. 47 oz (2 lb 15 oz) 2.94 lb (1.332 kg), West Des Moines, IA
    Reason, in FDA's words
    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
    Codes on the package
    Best if Used by Dates: 04-23-2017 thru 07-26-2017
    Where it was sold
    The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
    Amount recalled
    419/4 pizzas/cases
    Status
    Ended Sep 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3390-2017
    View in FDA's recall database
  9. ENDEDClass II · ModerateRecalled Jul 22, 2017

    Hy-Vee, Cheese Pizza, 12'' Thin Crust, UPC 288914 908999, Net Wt. 17 oz (1 lb 1 oz) 1.06 lb (482 g),...

    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list

    D & D Foods, Inc. · Omaha, NE

    Where it was sold: The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.

    UPC 288914908999
    Show details
    Product, as FDA describes it
    Hy-Vee, Cheese Pizza, 12'' Thin Crust, UPC 288914 908999, Net Wt. 17 oz (1 lb 1 oz) 1.06 lb (482 g), West Des Moines, IA
    Reason, in FDA's words
    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
    Codes on the package
    Best if Used by Dates: 04-23-2017 thru 07-26-2017
    Where it was sold
    The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
    Amount recalled
    182/4 pizzas/cases
    Status
    Ended Sep 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3391-2017
    View in FDA's recall database
  10. ENDEDClass II · ModerateRecalled Jul 22, 2017

    Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Net Wt. 29 oz (1 lb 13 oz) 1.81 lb (822 g)...

    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list

    D & D Foods, Inc. · Omaha, NE

    Where it was sold: The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.

    UPC 288942611991
    Show details
    Product, as FDA describes it
    Hy-Vee, Cheese Pizza, 16'' Thin Crust, UPC 288942 611991, Net Wt. 29 oz (1 lb 13 oz) 1.81 lb (822 g), West Des Moines, IA
    Reason, in FDA's words
    Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list
    Codes on the package
    Best if Used by Dates: 04-23-2017 thru 07-26-2017
    Where it was sold
    The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.
    Amount recalled
    119/4 pizzas/cases
    Status
    Ended Sep 7, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3392-2017
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Jul 21, 2017

    Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in...

    Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.

    Professional Complementary Health Formulas, LLC · Lake Oswego, OR

    Where it was sold: distributed in AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MT, NC, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, WA, and WI and in the following count...

    Show details
    Product, as FDA describes it
    Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic bottles. Adhesive label with White, black red and green print; bottle has a heat-shrink band. UPC code 8 40851 10054 0.
    Reason, in FDA's words
    Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
    Codes on the package
    Lot numbers: 409017; 503019; 508060; 603032; and 701039. QR Codes: 1409002; 1505019; 1603007; 1607022; and 1701013. QR codes are interpreted as below: " The first two digits represent the year in which the product was ordered or manufactured; " The second two digits represent the month in which the product was ordered or manufactured; and " The last three digits represent the products place in a sequential list of products ordered during that month and year.
    Where it was sold
    distributed in AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MT, NC, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, WA, and WI and in the following countries: Canada and United Kingdom
    Amount recalled
    2178/60 tablets Bottles
    Status
    Ended Mar 21, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3348-2017
    View in FDA's recall database
  12. ENDEDClass III · Low riskRecalled Jul 20, 2017

    "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Pa...

    Grandmas Herbs Cholesterol has undeclared soy lecithin.

    Grandma's Herbs · Saint George, UT

    Where it was sold: Nationwide. No foreign/military/govt accounts.

    UPC 714938000468
    Show details
    Product, as FDA describes it
    "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Packaging: PET plastic bottles, UPC# 714938 00046
    Reason, in FDA's words
    Grandmas Herbs Cholesterol has undeclared soy lecithin.
    Codes on the package
    Lot 13112
    Where it was sold
    Nationwide. No foreign/military/govt accounts.
    Amount recalled
    841 Bottles
    Status
    Ended Dec 19, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3409-2017
    View in FDA's recall database
  13. ENDEDClass I · Most seriousRecalled Jul 19, 2017

    Pumpkin Seeds, Blackened Seasoned 10 LB

    Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up with tree nuts (almonds and cashews).

    TRULY GOOD FOODS · Charlotte, NC

    Where it was sold: Nationwide

    Show details
    Product, as FDA describes it
    Pumpkin Seeds, Blackened Seasoned 10 LB
    Reason, in FDA's words
    Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up with tree nuts (almonds and cashews).
    Codes on the package
    lot # 15717
    Where it was sold
    Nationwide
    Amount recalled
    66 cases
    Status
    Ended May 20, 2019 (FDA lists it as terminated)
    FDA recall number
    F-3335-2017
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Jul 12, 2017

    STUTZMAN FARMS Organic Spelt Berries 25 lb 11.4 kg 6197

    The firm failed to include "wheat" in their allergen statement.

    Stutzman Farms · Millersburg, OH

    Where it was sold: Product was shipped to the following states: IN, KY, OH & PA

    Show details
    Product, as FDA describes it
    STUTZMAN FARMS Organic Spelt Berries 25 lb 11.4 kg 6197
    Reason, in FDA's words
    The firm failed to include "wheat" in their allergen statement.
    Codes on the package
    Sell By 6/19/2017 7/7/2018
    Where it was sold
    Product was shipped to the following states: IN, KY, OH & PA
    Amount recalled
    25/25 lb bags & 8/50 lb bags
    Status
    Ended Jul 24, 2020 (FDA lists it as terminated)
    FDA recall number
    F-3393-2017
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Jul 12, 2017

    STUTZMAN FARMS Savory Sprouted Spelt Crackers Net Wt. .30 LB. (136 g)

    The firm failed to include "wheat" in their allergen statement.

    Stutzman Farms · Millersburg, OH

    Where it was sold: Product was shipped to the following states: IN, KY, OH & PA

    Show details
    Product, as FDA describes it
    STUTZMAN FARMS Savory Sprouted Spelt Crackers Net Wt. .30 LB. (136 g)
    Reason, in FDA's words
    The firm failed to include "wheat" in their allergen statement.
    Codes on the package
    Sell By10/28/2017 & 11/5/2017
    Where it was sold
    Product was shipped to the following states: IN, KY, OH & PA
    Amount recalled
    8 cs/12/.30 lb bags
    Status
    Ended Jul 24, 2020 (FDA lists it as terminated)
    FDA recall number
    F-3394-2017
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Jul 10, 2017

    Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs poly bags. UPC for 2 lbs. package is 8 ...

    Undeclared wheat. Sooji Coarse is recalled because product contains Semolina but wheat is not declared on label.

    Reshmi's Group Inc. · Tukwila, WA

    Where it was sold: distributed in ID, OR and WA.

    Show details
    Product, as FDA describes it
    Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs poly bags. UPC for 2 lbs. package is 8 46499 00316 1 UPC for 4 lbs. package is 8 46499 00186 5. The label is read in parts: "***Ingredients: Sooji Coarse***Siva's***LOW FAT, GOOD SOURCE OF IRON, SOURCE OF FIBER, CHOLESTEROL FREE***Imported & Marketed by Reshmi's Group, Inc 6845 S. 220th ST KENT, WA 98032***".
    Reason, in FDA's words
    Undeclared wheat. Sooji Coarse is recalled because product contains Semolina but wheat is not declared on label.
    Codes on the package
    none
    Where it was sold
    distributed in ID, OR and WA.
    Amount recalled
    30 cases (20/2 lbs. package per case) AND 32 cases (10/4 lbs. packages per case)
    Status
    Ended Jun 18, 2018 (FDA lists it as terminated)
    FDA recall number
    F-0305-2017
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Jul 10, 2017

    Silver Star Tex-Mex Style Chipotle Queso Medium Dip Net Wt 16 OZ (1 Lb) packaged in a glass jar

    Undeclared milk (from cheese) and eggs.

    Texas Legend Foods · Austin, TX

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

    Where it was sold: USA

    Show details
    Product, as FDA describes it
    Silver Star Tex-Mex Style Chipotle Queso Medium Dip Net Wt 16 OZ (1 Lb) packaged in a glass jar
    Reason, in FDA's words
    Undeclared milk (from cheese) and eggs.
    Codes on the package
    Lots - 060AFV7A, 072AFV7A, 072AFV7B, 090AFV7A, 111AFV7A
    Where it was sold
    USA
    Amount recalled
    1537 cases
    Status
    Ended Oct 23, 2017 (FDA lists it as terminated)
    FDA recall number
    F-3337-2017
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled Jul 8, 2017

    Whole Foods Market PB & J Parfait Made With Greek Yogurt; Net Wt 8 OZ.;

    Sunneel Health Foods received a call from their customer indicating some of their Vegan Match Cocoa Parfaits were misbranded as PB & J Parfaits. The i...

    Sunneen Health Foods, LLC · Allentown, PA

    Where it was sold: NJ, NY

    Show details
    Product, as FDA describes it
    Whole Foods Market PB & J Parfait Made With Greek Yogurt; Net Wt 8 OZ.;
    Reason, in FDA's words
    Sunneel Health Foods received a call from their customer indicating some of their Vegan Match Cocoa Parfaits were misbranded as PB & J Parfaits. The ingredient statement failed to declare Soy, Almonds and Coconut allergens.
    Codes on the package
    Expiration date 7/13/17
    Where it was sold
    NJ, NY
    Amount recalled
    30 units
    Status
    Ended Jan 26, 2018 (FDA lists it as terminated)
    FDA recall number
    F-3350-2017
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Jul 6, 2017

    BioHealth Pasture Fed Precision Blend Time Release Protein: Cookies and Cream Flavor; Sold in 2 lb....

    Product contains undeclared wheat.

    Innovative Nutrition Technologies · San Dimas, CA

    Where it was sold: GA, LA, IL, AL, CO, CA, TX, IL, FL, AZ, WI, MD, OH, ID, NC, OK, NV, MO,

    UPC 642014594467UPC 642014594474
    Show details
    Product, as FDA describes it
    BioHealth Pasture Fed Precision Blend Time Release Protein: Cookies and Cream Flavor; Sold in 2 lb.(960G) UPC 6 42014 59446 7 and 4 lb. (1,920G) UPC 6 42014 59447 4 white plastic containers.
    Reason, in FDA's words
    Product contains undeclared wheat.
    Codes on the package
    2 lb.: 16041-F501-12417-02 - Expiry May 2019; 16041-F501-06517-02 - Expiry March 2019; 16041-F501-06517-03 - Expiry March 2019; 16041-F501-09617-01 - Expiry April 2019. 4 lb.; 16041-F501-10317-01 - Expiry April 2019; 16041-F501-10317-02 - Expiry April 2019; 16041-F501-12417-02 - Expiry May 2019; 16041-F501-1217-01 - Expiry May 2019 16041-F501-06517-01 - Expiry March 2019; 16041-F501-06517-02 - Expiry March 2019; 16041-F501-18217-01 - Expiry June 2019; 16041-F501-16017-01 - Expiry June 2019.
    Where it was sold
    GA, LA, IL, AL, CO, CA, TX, IL, FL, AZ, WI, MD, OH, ID, NC, OK, NV, MO,
    Amount recalled
    1139 x 4 lb and 1351 x 2 lb. containers
    Status
    Ended Aug 29, 2017 (FDA lists it as terminated)
    FDA recall number
    F-2888-2017
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Jul 6, 2017

    Fudge Brownie, Net Wt. 9 oz. (0.6 lb.) (255g), with the following brands: 1. Cashwise Gluten Free B...

    Some Gluten Free Chocolate Chip Bars were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Chocolate Chip Bars that are incorrectly...

    Coborn's, Inc · Saint Cloud, MN

    Where it was sold: MN, ND, SD, WI

    Show details
    Product, as FDA describes it
    Fudge Brownie, Net Wt. 9 oz. (0.6 lb.) (255g), with the following brands: 1. Cashwise Gluten Free Bakery, 2. Coborn's Gluten Free Bakery.
    Reason, in FDA's words
    Some Gluten Free Chocolate Chip Bars were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Chocolate Chip Bars that are incorrectly labeled as Gluten Free Fudge Brownies do contain milk.
    Codes on the package
    Expiration date of July 10, 2017
    Where it was sold
    MN, ND, SD, WI
    Amount recalled
    122 packages
    Status
    Ended Aug 1, 2019 (FDA lists it as terminated)
    FDA recall number
    F-3351-2017
    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.