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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

610 recalls · showing 301 to 320

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  1. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3, 60 softgels per bottle, UPC 7 05875 61...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875610056
    Show details
    Product, as FDA describes it
    Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3, 60 softgels per bottle, UPC 7 05875 61005 6.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    32 bottles
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1361-2019
    View in FDA's recall database
  2. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10085, Barleans, Ultra EPA-DHA Fish Oil 1,300 mg Omega-3 Orange Flavor, 60 Softgels per bott...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875610063
    Show details
    Product, as FDA describes it
    Item FG 10085, Barleans, Ultra EPA-DHA Fish Oil 1,300 mg Omega-3 Orange Flavor, 60 Softgels per bottle. UPC 7 05875 61006 3.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    229 bottles
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1362-2019
    View in FDA's recall database
  3. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10089, Barlean s, Fish Oil Omega-3 EPA/DHA Orange Flavor, 100 Softgels per bottle. UPC 7 05...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875610070UPC 705875610087
    Show details
    Product, as FDA describes it
    Item FG 10089, Barlean s, Fish Oil Omega-3 EPA/DHA Orange Flavor, 100 Softgels per bottle. UPC 7 05875 61007 0. Item FG 10090, Barlean s, Fish Oil Omega-3 EPA/DHA Orange Flavor, 250 Softgels per bottle. UPC 7 05875 61008 7.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    1845 bottles (FG 10089); 3606 bottles (FG 10090)
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1363-2019
    View in FDA's recall database
  4. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels per bottle. UPC 7 05875 70009 2. Item ...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875700092UPC 705875000857
    Show details
    Product, as FDA describes it
    Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels per bottle. UPC 7 05875 70009 2. Item FG 10107, Barlean s, Olive Leaf Complex, 60 Softgels per bottle. UPC 7 05875 0008 5.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    239 bottles (FG 10106) and 1565 bottles (FG 10107)
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1364-2019
    View in FDA's recall database
  5. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10116, Barlean s, Master Blend Total Omega 3.6.9 Lemonade Flavor, 90 Softgels per bottle. UP...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875100205
    Show details
    Product, as FDA describes it
    Item FG 10116, Barlean s, Master Blend Total Omega 3.6.9 Lemonade Flavor, 90 Softgels per bottle. UPC 7 05875 10020 5.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    1943 bottles
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1365-2019
    View in FDA's recall database
  6. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10146, Barlean s, Essential Woman, 120 count Softgels per bottle, UPC 7 05875 10013 7. I...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875100137UPC 705875100090
    Show details
    Product, as FDA describes it
    Item FG 10146, Barlean s, Essential Woman, 120 count Softgels per bottle, UPC 7 05875 10013 7. Item FG 10147, Barlean s, Essential Woman, 60 count Softgels per bottle, UPC 7 05875 10009 0.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    1144 bottles (FG 10146) and 1913 bottles (FG 10147)
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1366-2019
    View in FDA's recall database
  7. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875100199
    Show details
    Product, as FDA describes it
    Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    1360 bottles
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1367-2019
    View in FDA's recall database
  8. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softgels per bottle. UPC 7 05875 80113 3. ...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875801133UPC 705875801157
    Show details
    Product, as FDA describes it
    Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softgels per bottle. UPC 7 05875 80113 3. Item FG 10193, Barleans Full Spectrum Hemp Extract, 30 Softgels per bottle. UPC 7 05875 80115 7.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2021 and earlier
    Where it was sold
    nationwide
    Amount recalled
    firm did not provide
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1368-2019
    View in FDA's recall database
  9. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875801126UPC 705875801140
    Show details
    Product, as FDA describes it
    Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per bottle. UPC 7 05875 80112 6. Item FG 10194, Barlean s Ideal CBD Hemp Oil softgel, 750 mg CBD, Less than 0.3% THC, 30 Softgels per bottle. UPC 7 05875 80114 0.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2021 and earlier
    Where it was sold
    nationwide
    Amount recalled
    589 bottles (FG 10191); did not provide for FG 10194
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1369-2019
    View in FDA's recall database
  10. ENDEDClass III · Low riskRecalled May 6, 2019

    Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle. UPC 7 05875 1007 6. Item FG 10081, Ba...

    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

    Barlean's Llc · Ferndale, WA

    Where it was sold: nationwide

    UPC 705875100762UPC 705875100083UPC 705875140041
    Show details
    Product, as FDA describes it
    Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle. UPC 7 05875 1007 6. Item FG 10081, Barleans, Lignan Flax Oil, 250 Softgels per bottle. UPC 7 05875 10008 3. Item FG 70000, Barlean's, Pure Flax Oil, 45 Softgels per bottle, label in English and Bulgarian. UPC 7 05875 14004 1.
    Reason, in FDA's words
    Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
    Codes on the package
    Best By of January 2022 and earlier
    Where it was sold
    nationwide
    Amount recalled
    667 bottles (Item FG 10079); 1058 bottles (FG 10081); Firm did not provide for FG 7000
    Status
    Ended Oct 15, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1371-2019
    View in FDA's recall database
  11. ENDEDClass III · Low riskRecalled May 1, 2019

    Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt: 5.25 ozs 150g Distributed by: U.S. Tra...

    Undeclared sulfites.

    U.S. Tov, Inc. · Hayward, CA

    Where it was sold: U.S. distribution to the following: AK, AR, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MI, MO, NC, NE, NM , NV, NY, OH, SC, TN, TX, UT, VA, WA, WI No foreign distribution.

    UPC 721557371152
    Show details
    Product, as FDA describes it
    Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt: 5.25 ozs 150g Distributed by: U.S. Trading Company Product of Thailand Item Number:37115 UPC: 721557371152
    Reason, in FDA's words
    Undeclared sulfites.
    Codes on the package
    Lot Number: 284PBH Expired 1/11/19 Lot Number: 345TBI Expires 11/02/19
    Where it was sold
    U.S. distribution to the following: AK, AR, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MI, MO, NC, NE, NM , NV, NY, OH, SC, TN, TX, UT, VA, WA, WI No foreign distribution.
    Amount recalled
    68 units
    Status
    Ended Jul 1, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1337-2019
    View in FDA's recall database
  12. ENDEDClass II · ModerateRecalled Apr 22, 2019

    Key Lime and Cream Torte, 5 oz., Keep in Freezer for up to 6 months or refrigerated for 5 days

    The product contains undeclared FD&C Colors Yellow #5 and Blue #1.

    Island Desserts Llc DBA Pastry Art · Walpole, MA

    Where it was sold: MA and RI

    Show details
    Product, as FDA describes it
    Key Lime and Cream Torte, 5 oz., Keep in Freezer for up to 6 months or refrigerated for 5 days
    Reason, in FDA's words
    The product contains undeclared FD&C Colors Yellow #5 and Blue #1.
    Codes on the package
    delivered after 10/18/2018
    Where it was sold
    MA and RI
    Amount recalled
    810 desserts, 5-oz. each
    Status
    Ended Jun 12, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1332-2019
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Mar 29, 2019

    Addback Tablet Dietary Supplement 60 tablets per 190cc Oblong WHDPE bottle Net Wet: 85gm (60 ta...

    Undeclared coating ingredients: HPMC, Triacetin, Titanium Dioxide, FD & C Yellow # 5, FD & C Yellow # 6, FD & C Blue # 1. In addition, the label state...

    Cays LLC · Southington, CT

    Where it was sold: All product is in the firm's possession.

    UPC 651536124526
    Show details
    Product, as FDA describes it
    Addback Tablet Dietary Supplement 60 tablets per 190cc Oblong WHDPE bottle Net Wet: 85gm (60 tablet wt) UPC- 0651536124526 Firm name Prevent D Labs Division of CAYS, LLC Southington, CT
    Reason, in FDA's words
    Undeclared coating ingredients: HPMC, Triacetin, Titanium Dioxide, FD & C Yellow # 5, FD & C Yellow # 6, FD & C Blue # 1. In addition, the label states Silicon Dioxide, which is not part of the formulation
    Codes on the package
    Code NS-1930F Lot # 1810553 Exp. Date 12/2020
    Where it was sold
    All product is in the firm's possession.
    Amount recalled
    2095 bottles
    Status
    Ended Jan 22, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1295-2019
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Mar 28, 2019

    Samira Food Products Vegeterian 100% Soy Chunk, Net Wt. 8oz

    Failure to declare sulfites.

    Traders West Inc · Medley, FL

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

    Where it was sold: Domestic distribution only.

    Show details
    Product, as FDA describes it
    Samira Food Products Vegeterian 100% Soy Chunk, Net Wt. 8oz
    Reason, in FDA's words
    Failure to declare sulfites.
    Codes on the package
    No lot or batch number.
    Where it was sold
    Domestic distribution only.
    Amount recalled
    48 units/8oz
    Status
    Ended Oct 9, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1306-2019
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Mar 25, 2019

    Rice Valley Ready Cooked Noodles and Instant Noodles, Net Wt, 14 oz. plastic bag - Perishable, Ke...

    FDA inspection at the facility found that the firm was using Yellow 5 & 6 which were not declared on product labeling.

    Rice Valley · San Francisco, CA

    Where it was sold: Bay area of California only.

    UPC 992320403053UPC 992304030152
    Show details
    Product, as FDA describes it
    Rice Valley Ready Cooked Noodles and Instant Noodles, Net Wt, 14 oz. plastic bag - Perishable, Keep Refrigerate UPC 9 92320 40305 3, UPC: 9 9230 40301 5 Made in USA Rice Valley Foods Company, San Francisco, CA 94124
    Reason, in FDA's words
    FDA inspection at the facility found that the firm was using Yellow 5 & 6 which were not declared on product labeling.
    Codes on the package
    0088
    Where it was sold
    Bay area of California only.
    Amount recalled
    335 Packs
    Status
    Ended Sep 25, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1322-2019
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Mar 1, 2019

    Snow's PREMIUM ICE CREAM Mint Chip Mint Ice Cream with Dark Chocolate Chunks 1.5 QUART (1.42L) KEEP ...

    Product contains undeclared Yellow #5.

    Snow's Acquisition, LLC · Greenfield, MA

    Where it was sold: MA

    Show details
    Product, as FDA describes it
    Snow's PREMIUM ICE CREAM Mint Chip Mint Ice Cream with Dark Chocolate Chunks 1.5 QUART (1.42L) KEEP FROZEN, UPCE: 0 48896400139
    Reason, in FDA's words
    Product contains undeclared Yellow #5.
    Codes on the package
    Lot Codes: 081920; 072020
    Where it was sold
    MA
    Amount recalled
    104 sleeves
    Status
    Ended Apr 1, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1230-2019
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Feb 25, 2019

    JOY NATURAL TAMARIND CONCENTRATE Net Wt.: 14FL OZ. (400g), UPC: 6 80617 60020 8 and Net Wt.: 32 FL O...

    Product contains undeclared sulfites.

    JOY GOURMET FOODS LLC · Maspeth, NY

    Where it was sold: CT, NY, NJ

    UPC 680617600208UPC 680617600215
    Show details
    Product, as FDA describes it
    JOY NATURAL TAMARIND CONCENTRATE Net Wt.: 14FL OZ. (400g), UPC: 6 80617 60020 8 and Net Wt.: 32 FL Oz. (915g) UPC: 6 80617 60021 5
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    0306, 0314, 0614, 0717, 01022, 01211 3/6/2019, 3/14/2019, 6/14/2019, 7/17/2019, 10/22/2019, 12/14/2019
    Where it was sold
    CT, NY, NJ
    Amount recalled
    unknown
    Status
    Ended Jul 10, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1212-2019
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Feb 25, 2019

    JOY Ginger Paste NET WT 26 OZ (737g), UPC: 6 80617 60001 7 and NET WT 8 OZ (228g), UPC: 6 80617 6000...

    Product contains undeclared sulfites.

    JOY GOURMET FOODS LLC · Maspeth, NY

    Where it was sold: CT, NY, NJ

    UPC 680617600017UPC 680617600024
    Show details
    Product, as FDA describes it
    JOY Ginger Paste NET WT 26 OZ (737g), UPC: 6 80617 60001 7 and NET WT 8 OZ (228g), UPC: 6 80617 60002 4
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    0226, 411, 0706, 0731, 01029 2/26/2019, 4/11/2019, 7/6/2019, 7/31/2019, 10/29/2019
    Where it was sold
    CT, NY, NJ
    Amount recalled
    unknown
    Status
    Ended Jul 10, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1213-2019
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Feb 25, 2019

    JOY Garlic Paste NET WT 26 OZ (737 g) UPC: 6 80617 60003 1 and NET WT 8 OZ (228g) UPC: 6 80617 60004...

    Product contains undeclared sulfites.

    JOY GOURMET FOODS LLC · Maspeth, NY

    Where it was sold: CT, NY, NJ

    UPC 680617600031UPC 680617600048
    Show details
    Product, as FDA describes it
    JOY Garlic Paste NET WT 26 OZ (737 g) UPC: 6 80617 60003 1 and NET WT 8 OZ (228g) UPC: 6 80617 60004 8
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    0227, 0425, 0709, 0813, 01106 2/27/2019, 4/25/2019, 7/9/2019, 8/13/2019, 11/6/2019
    Where it was sold
    CT, NY, NJ
    Amount recalled
    unknown
    Status
    Ended Jul 10, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1214-2019
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Feb 25, 2019

    JOY GOL-GAPPA (PANI PURI) MASALA CONCENTRATE, NET WT 8 OZ (228g), UPC: 6 80617 60414 5

    Product contains undeclared sulfites.

    JOY GOURMET FOODS LLC · Maspeth, NY

    Where it was sold: CT, NY, NJ

    UPC 680617604145
    Show details
    Product, as FDA describes it
    JOY GOL-GAPPA (PANI PURI) MASALA CONCENTRATE, NET WT 8 OZ (228g), UPC: 6 80617 60414 5
    Reason, in FDA's words
    Product contains undeclared sulfites.
    Codes on the package
    0712 7/12/2019
    Where it was sold
    CT, NY, NJ
    Amount recalled
    unknown
    Status
    Ended Jul 10, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1215-2019
    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.