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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

28,406 ended recalls · showing 861 to 880

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  1. ENDEDClass III · Low riskRecalled Aug 6, 2025

    FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PR...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    Show details
    Product, as FDA describes it
    FORMUTECH NUTRITION FLEXIBLE JOINT FORMULA WITH CISSUS QUADRANGULARIS SUPPORTS TENDONS & MUSSCLES PROMOTES HEALTH CARTILAGE LUBRICATES JOINTS 240 Capsules UPC 7 97573 90884 1 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot 405310805 Exp Date 07/28
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0586-2025
    View in FDA's recall database
  2. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS ADDEREX XR STRONGEST FOCUSING AID WITHOUT A PRESECRIPTION! HELPS ADULTS MAIN...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811836026917
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS ADDEREX XR STRONGEST FOCUSING AID WITHOUT A PRESECRIPTION! HELPS ADULTS MAINTAIN CONCENTRATION & IMPROVE PRODUCTIVITY! 30 TABLETS UPC 8 11836 02691 7 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot 303120691 Exp Date 05/28
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0587-2025
    View in FDA's recall database
  3. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED PHYTOSTEROL 99%) PROVIDES SUPPORT FOR OV...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811836025873
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED PHYTOSTEROL 99%) PROVIDES SUPPORT FOR OVERALL CARDIOVASCULAR HEALTH HELPS MAINTAIN HEALTHY CHOLESTEROL LEVELS ALREADY WITHIN THE NORMAL RANGE SUPPORTS PROSTATE AND IMMUNE HEALTH 90 TABLETS UPC 8 11836 02587 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot C1847 Exp Date 05/29
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0588-2025
    View in FDA's recall database
  4. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS FISH OIL HEART AND BRAIN HEALTH EPA/DHA OMEGA 3 FATTY ACIDS SUPPORTS CARDIOV...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811836025859
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS FISH OIL HEART AND BRAIN HEALTH EPA/DHA OMEGA 3 FATTY ACIDS SUPPORTS CARDIOVASCULAR HEALTH MAY HELP WITH JOINT PAIN MAY IMPROVE COGNITIVE FUNCTION 90 SOFT GELS UPC 8 11836 02585 9 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot 517120551 Exp Date 04/30
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0589-2025
    View in FDA's recall database
  5. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolu...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 857084000354
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity Dr Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot 503110607 Exp Date 04/30
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0590-2025
    View in FDA's recall database
  6. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION M...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811836023626
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH PHARMECEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot 059960809 Exp Date 06/28
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0591-2025
    View in FDA's recall database
  7. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CIRCULATION SUPPORTS CARDIOVASCULAR HEALTH...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811836024463
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS PINE BARK SUPPORTS HEART HEALTH & CIRCULATION SUPPORTS CARDIOVASCULAR HEALTH FIGHTS OXIDATIVE STRESS 60 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02446 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot C15Cl4 Exp Date 10/26
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0592-2025
    View in FDA's recall database
  8. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST AND SECRETAGOGUES NOVEL GIP (GLUCOSE-DEPENDENT ISNULINOTROPIC POLYPEPTIDE) RECEPTOR AGONIST 180 TABLETS DIETARY SUPPLEMENT
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot C19El8 Exp Date 05/30
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0593-2025
    View in FDA's recall database
  9. ENDEDClass III · Low riskRecalled Aug 6, 2025

    HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CAR...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811836024913
    Show details
    Product, as FDA describes it
    HI-TECH PHARMACEUTICALS QUERCETIN STRENGTHENS IMMUNE SYSTEM SUPPORTS RESPIRATORY HEALTH SUPPORTS CARDIOVASCULAR HEALTH 120 TABLETS DIETARY SUPPLEMENT UPC 8 11836 02491 3 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot C1612 Exp Date 08/27
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0594-2025
    View in FDA's recall database
  10. ENDEDClass III · Low riskRecalled Aug 6, 2025

    IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS DIETARY SUPPLEMENT 120 CAPSULES UPC 8 54...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 854503002265
    Show details
    Product, as FDA describes it
    IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS DIETARY SUPPLEMENT 120 CAPSULES UPC 8 54503 00226 5 Manufactured By: iForce Nutrition 6015B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot 101330812 Exp Date 01/25
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0595-2025
    View in FDA's recall database
  11. ENDEDClass III · Low riskRecalled Aug 6, 2025

    LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH PCT LEGAL GEAR DIETARY SUPPLEM...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 744890941516
    Show details
    Product, as FDA describes it
    LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH PCT LEGAL GEAR DIETARY SUPPLEMENT 17-PROANDRO pBOLD FORM-XT UPC 7 44890 94151 6 MADE FOR LG SCIENCES 6015-B UNITY DR. NORCROXX, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot Cl 78216691877 Exp Date 02/28
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0596-2025
    View in FDA's recall database
  12. ENDEDClass III · Low riskRecalled Aug 6, 2025

    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENE...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 689466706192
    Show details
    Product, as FDA describes it
    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT KIWI-STRAWBERRY NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 89466 70619 2 Manufactured by: Prime Nutrition 6015-b Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot 207460659 Exp Date 10/25
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0597-2025
    View in FDA's recall database
  13. ENDEDClass III · Low riskRecalled Aug 6, 2025

    PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS ENERGY PRODUCTION PROTEN ...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 689466706017
    Show details
    Product, as FDA describes it
    PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 SERVINGS SUPPORTS ENERGY PRODUCTION PROTEN ANTIOXIDANT PROPERTIES SUPPORTS HEALTHY BLOOD SUGAR LEVELS NET WT. 8.12OZ (250g) DIETARY SUPPLEMENT UPC 6 89466 70601 7 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot 710581618 Exp Date 12/26
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0598-2025
    View in FDA's recall database
  14. ENDEDClass III · Low riskRecalled Aug 6, 2025

    Top Secret Nutrition extra strength uric control fast acting multi-pronged uric acid control 30 vegg...

    Unapproved Drug Claims.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 811226021584
    Show details
    Product, as FDA describes it
    Top Secret Nutrition extra strength uric control fast acting multi-pronged uric acid control 30 veggie caps DIETARY SUPPLEMENT UPC 8 11226 02158 4 Distributed by: TOP SECRET NUTRITION, LLC 6015-B Unity Dr. Norcross, GA 30052
    Reason, in FDA's words
    Unapproved Drug Claims.
    Codes on the package
    Lot C1238 Exp Date 01/25
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0599-2025
    View in FDA's recall database
  15. ENDEDClass III · Low riskRecalled Aug 6, 2025

    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENE...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 638302409063
    Show details
    Product, as FDA describes it
    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT PEACH MANGO NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40906 3 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot 202140114 Exp Date 03/27
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0600-2025
    View in FDA's recall database
  16. ENDEDClass III · Low riskRecalled Aug 6, 2025

    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENE...

    Unapproved Drug Claims and Misbranded.

    Hi-Tech Pharmaceuticals Inc. · Norcross, GA

    Where it was sold: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH,...

    UPC 638302409056
    Show details
    Product, as FDA describes it
    PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT WATERMELON NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEMENT UPC 6 38302 40905 6 Manufactured by: Prime Nutrition 6015-B Unity Drive Norcross, GA 30071
    Reason, in FDA's words
    Unapproved Drug Claims and Misbranded.
    Codes on the package
    Lot 174271126 Exp Date 09/26
    Where it was sold
    Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
    Amount recalled
    85,950 units total
    Status
    Ended Feb 19, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0601-2025
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Aug 5, 2025

    Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noo...

    Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.

    Kobayashi Noodle U.S.A. · Gardena, CA

    Where it was sold: CA

    Show details
    Product, as FDA describes it
    Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
    Reason, in FDA's words
    Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
    Codes on the package
    Lots: 911, 916, 919, 932, 935, 940, 945, 950
    Where it was sold
    CA
    Amount recalled
    945 cases
    Status
    Ended Apr 6, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0502-2025
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Aug 5, 2025

    Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noo...

    Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.

    Kobayashi Noodle U.S.A. · Gardena, CA

    Where it was sold: CA

    Show details
    Product, as FDA describes it
    Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (4942) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
    Reason, in FDA's words
    Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
    Codes on the package
    Lot#893, Lot#894, Lot#897, Lot#898, Lot#899, Lot#900, Lot#901, Lot#902, Lot#903, Lot#904, Lot#905, Lot#906, Lot#907, Lot#910, Lot#912, Lot#913, Lot#914, Lot#915, Lot#916, Lot#917, Lot#918, Lot#921, Lot#922, Lot#923, Lot#924, Lot#925, Lot#926, lot#927, Lot#928, Lot#929, Lot#930, Lot#933, Lot#934, Lot#936, Lot#937, Lot#938, Lot#939, Lot#940, Lot#942, Lot#943, Lot#946, Lot#947, Lot#948, Lot#949, Lot#951
    Where it was sold
    CA
    Amount recalled
    2800 cases
    Status
    Ended Apr 6, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0503-2025
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Aug 5, 2025

    Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. ...

    Imported Frozen Oyster potentially contaminated with Norovirus.

    Khee Trading, Inc. · Compton, CA

    Where it was sold: Distribution is 8 distributor consignees across California, NV, AZ and TX.

    Show details
    Product, as FDA describes it
    Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side panel reads: Method of harvest: Farm Raised Country of Origin: Republic of Korea ICSSL NO: KR-15-SP No UPC
    Reason, in FDA's words
    Imported Frozen Oyster potentially contaminated with Norovirus.
    Codes on the package
    B250123
    Where it was sold
    Distribution is 8 distributor consignees across California, NV, AZ and TX.
    Amount recalled
    828 cartons
    Status
    Ended Jul 21, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0520-2025
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Aug 5, 2025

    Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. ...

    Imported Frozen Oyster potentially contaminated with Norovirus.

    Khee Trading, Inc. · Compton, CA

    Where it was sold: Distribution is 8 distributor consignees across California, NV, AZ and TX.

    Show details
    Product, as FDA describes it
    Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side panel reads: Method of harvest: Farm Raised Country of Origin: Republic of Korea ICSSL NO: KR-15-SP No UPC
    Reason, in FDA's words
    Imported Frozen Oyster potentially contaminated with Norovirus.
    Codes on the package
    B250112
    Where it was sold
    Distribution is 8 distributor consignees across California, NV, AZ and TX.
    Amount recalled
    98 cartons
    Status
    Ended Jul 21, 2026 (FDA lists it as terminated)
    FDA recall number
    H-0521-2025
    View in FDA's recall database

Show more recalls

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.