The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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551–575 of 810

  • CriticalFDA (Drugs)·D-0881-2016·2016-06-01

    FDA Recalls Weight Loss Product Containing Undeclared Sibutramine and Phenolphthalein

    Lucy's Weight Loss System is recalling Shorts on The Beach Golden Edition because it contains undeclared sibutramine and phenolphthalein.

    Product
    Shorts on The Beach Golden Edition by Pink Bikini, 800 mg, packaged in 30-count plastic bottle, Manufactured and Distributed by: Lucy's Weight Loss System, Arlington, Texas 76010
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0860-2016·2016-06-01

    Lipo Escultura capsules recalled for containing unapproved prescription drugs

    Lipo Escultura capsules are being recalled because they contain sibutramine and diclofenac, making them unapproved drugs rather than dietary supplements.

    Product
    LIPO ESCULTURA capsules, 250 mg, 60-count bottles, Distributed By: JAT Productos Naturales Corp., BROOKLYN, NY 11238, www.lipoesculturatreatment.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0882-2016·2016-06-01

    Pink Bikini capsules recalled for undeclared dangerous ingredients

    Lucy's Weight Loss System is recalling Pink Bikini capsules because they contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac.

    Product
    Pink Bikini capsules, (all colors and all strengths), packaged in 30-count bottle, Manufactured and Distributed by: Lucy's Weight Loss System (dba Waisted With Lucy), Arlington, TX 76010
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0869-2016·2016-06-01

    Avastin Syringes Recalled for Bacterial Contamination

    AmEx Pharmacy is recalling 45 Avastin syringes nationwide because testing revealed bacterial contamination.

    Product
    Avastin (Bevacizumab) 2 mg/0.08 mL syringe, Office Administration Only, AmEx Pharmacy, 1515 Elizabeth St Suite J, Melbourne, FL 32901.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0908-2016·2016-06-01

    Licorice Coughing Liquid Recalled for Undeclared Morphine

    Master Herbs is recalling Licorice Coughing Liquid because it contains undeclared morphine and was marketed without an approved NDA or ANDA.

    Product
    Licorice Coughing Liquid (guaifenesin), 5%, 3.38 fl. oz. (100 ml), OTC, Manufactured by: Ma Ying Long Pharmaceutical Group Co., LTD, Wuhan, China; Distributed by: Master Herbs (USA) Inc., NDC 68511-0460-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0883-2016·2016-06-01

    Shorts on the Beach capsules recalled for undeclared dangerous ingredients

    Lucy's Weight Loss System is recalling Shorts on the Beach capsules because they contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac.

    Product
    Shorts on the Beach capsules, (all colors and all strengths), packaged in 30-count bottle, Manufactured and Distributed by: Lucy's Weight Loss System (dba Waisted With Lucy), Arlington, TX 76010
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0880-2016·2016-06-01

    FDA Recalls Weight Loss Capsules Containing Undeclared Sibutramine and Phenolphthalein

    Lucy's Weight Loss is recalling Shorts on The Beach Strong Formula capsules nationwide because they contain undeclared sibutramine and phenolphthalein.

    Product
    Shorts on The Beach Strong Formula by Pink Bikini capsules, 750 mg, packaged in 30-count plastic bottle, Manufactured and Distributed by: Lucy's Weight Loss System, Arlington, Texas 76010
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0771-2016·2016-03-16

    Tf Supplements Recalls Rhino 7 3000 Due to Undeclared Ingredients

    Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.

    Product
    RHINO 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0772-2016·2016-03-16

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.

    Product
    Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA, UPC 700729253748
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-724-2016·2016-02-24

    Pharmedium Recalls Subpotent Fentanyl Citrate Syringes for IV Use

    Pharmedium Services, LLC is recalling 500 syringes of fentanyl citrate because the drug was subpotent. The affected product was distributed to nine hospital pharmacies.

    Product
    fentaNYL Citrate, Preservative Free, 10 mcg per 1 mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3174, PharMEDium
    Category
    Drug
    Distribution
    7 states
  • CriticalFDA (Drugs)·D-0668-2016·2016-02-24

    Hospira Recalls Magnesium Sulfate Injection Bags Due to Incorrect Barcode Labeling

    Hospira is recalling 213,600 bags of Magnesium Sulfate in Water for Injection because the primary bag labeling may be mislabeled with a barcode that scans as heparin sodium.

    Product
    MAGNESIUM SULFATE IN WATER — MAGNESIUM SULFATE IN WATER (MAGNESIUM SULFATE IN WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0669-2016·2016-02-24

    Glades Drugs Recalls Vitamin D3 Supplement Due to Excessive Potency

    Glades Drugs Inc. is recalling Vitamin D3 supplement capsules because they contain an extremely high level of vitamin D3.

    Product
    Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylcobalamin/pyridoxine/methionine/inositol/choline bitartrate USP) capsules, 60, 120 or 180 count vials, Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476.
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0673-2016·2016-02-24

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    FDA recalls Rhino 7 Platinum 3000 because it contains undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.

    Product
    Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0671-2016·2016-02-24

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000 single blister packs because they contain undeclared active pharmaceutical ingredients.

    Product
    Rhino 7 Platinum 3000, Single Blister Packs, distributed By Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0670-2016·2016-02-24

    Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients

    MSNV, Inc dba National Video Supply is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients.

    Product
    Rhino 7 3000, 6 count bottles, Distributed by Rhino 7, Made in USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0674-2016·2016-02-24

    Medisca Recalls L-Citrulline API Due to Labeling Error

    Medisca Inc is recalling L-Citrulline API bottles because FDA testing found the product contained N-acetyl-leucine instead of the labeled ingredient.

    Product
    CITRULLINE (L) in 25 g, 100 g, 500 g and 1 kg plastic bottles, White crystals or crystalline powder, odorless, For Use and distribution in prescription compounding, manufacturing, processing, or repackaging only in accordance with FDA regulations and applicable law, Packaged by M
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0672-2016·2016-02-24

    Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients

    Premiere Sales Group is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.

    Product
    Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0675-2016·2016-02-24

    Inaffit Recalls Natureal Burn Fat Nature Due to Undeclared Sibutramine

    Inaffit, LLC is recalling Natureal Burn Fat Nature capsules because the product contains undeclared sibutramine and was marketed without an approved NDA or ANDA.

    Product
    NATUREAL BURN FAT NATURE, 30-count capsules, packaged in clear plastic bottle, Manufactured for: Inaffit, LLC. P.O. Box 34056, Bethesda, MD 20827.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0722-2016·2016-02-24

    Fit Firm and Fabulous Recalls Ultimate Herbal Slimcap Capsules

    Fit Firm and Fabulous is recalling Ultimate Herbal Slimcap Capsules because they contain undeclared sibutramine, a controlled substance removed from the U.S. market for safety reasons.

    Product
    Ultimate Herbal Slimcap Capsules, 350 mg*, 30-count bottles, labeled Part 1 of 3, fit firm & fabulous, UPC 5 42423 25422 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0662-2016·2016-02-24

    Medline Recalls Mislabeled Acetaminophen Extra-Strength Pain Reliever Tablets

    Medline Industries is recalling 500 mg acetaminophen tablets mislabeled as 325 mg. Consumers should stop using the product and return it to the retailer.

    Product
    ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets, 500 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-641-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0664-2016·2016-02-24

    Akttive Fat Burner Recalled for Undeclared Dangerous Ingredients

    Life and More LLC is recalling Akttive High Performance Fat Burner Gold capsules because FDA testing found undeclared sibutramine, desmethylsibutramine, and phenolphthalein.

    Product
    Akttive High Performance Fat Burner Gold dietary supplement capsules, 30-count bottle, Distributed by Life and More, L.L.C., Doral, Florida
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-723-2016·2016-02-24

    Pharmedium Recalls Subpotent Fentanyl Citrate Syringes for IV Use

    Pharmedium Services, LLC is recalling 180 syringes of fentanyl citrate because the drug was subpotent. The affected product was distributed to nine hospital pharmacies.

    Product
    fentaNYL Citrate, Preservative Free, 5 mcg per mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3479, PharMEDium.
    Category
    Drug
    Distribution
    7 states
  • CriticalFDA (Drugs)·D-0667-2016·2016-02-24

    APEXXX tablets recalled for containing unapproved sildenafil

    Nuway Distributors is recalling APEXXX tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.

    Product
    APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0297-2016·2015-11-25

    KABOOM Action Strips Recalled for Undeclared Sulfoaildenafil

    Blue Square Market, Inc. is recalling KABOOM action strips because they contain undeclared sulfoaildenafil and were marketed without an approved NDA or ANDA.

    Product
    KABOOM action strips, Sexual Performance Strips, packaged in 6.4oz box 12 strips per box, Nutrology USA LLC
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0296-2016·2015-11-25

    LiDa DAIDAIHUA capsules recalled for undeclared sibutramine and phenolphthalein

    Blue Square Market, Inc. is recalling LiDa DAIDAIHUA capsules nationwide because they contain undeclared sibutramine and phenolphthalein and were marketed without an approved NDA or ANDA.

    Product
    LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG), capsules, packaged in 1.6oz box 30 capsules per box, Kunming Dali Industry & Trade Co., Ltd
    Category
    Drug
    Distribution
    Distributed nationwide