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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776–800 of 840

  • CriticalFDA (Drugs)·D-1045-2014·2014-02-05

    FDA Recalls Rhino 5 Capsules Containing Unapproved Drug Ingredients

    FDA is recalling Rhino 5 capsules marketed as a dietary supplement because they contain undeclared desmethyl carbondenafil and dapoxetine, making them unapproved new drugs.

    Product
    Rhino 5 capsules(Spanish & English Labeling), 1 capsule per blister pack, Distributed by P&A Enterprise, Buena Park, CA 90621, English UPC 6 10708 10730 9, Spanish UPC 6 10708 10729 3.
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1052-2014·2014-02-05

    NuVision Pharmacy Recalls Sermorelin/GHRP-6 Vials Due to Sterility Concerns

    NuVision Pharmacy is recalling 122 vials of Sermorelin/GHRP-6 due to lack of sterility assurance identified during an FDA inspection.

    Product
    Sermorelin/GHRP-6, 3 mg/3 mg, 5 mL vial, Stock # 21740, Compounded by NuVision Pharmacy, Dallas, TX 75244
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1046-2014·2014-02-05

    MaXtremeZEN Capsules Recalled for Containing Unapproved Drug Ingredients

    SS Wholesale Inc. is recalling MaXtremeZEN capsules because FDA analysis found undeclared desmethyl carbondenafil and dapoxetine, making the product an unapproved new drug.

    Product
    MaXtremeZEN capsules, 1 capsule per blister pack, Distributed by: P&A Enterprise, Buena Park, CA 90621, UPC 6 10079 52468 2.
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1050-2014·2014-02-05

    FDA Recalls Hydravax Weight Loss Supplement for Undeclared Prescription Drug

    IQ Formulations is recalling Hydravax High Potency Diuretic Weight Loss Solution because it contains an undeclared prescription diuretic, Triamterene.

    Product
    Hydravax High Potency Diuretic Weight Loss Solution, Pharmaceutical Grade, 45 capsules per bottle, Dietary Supplement, Manufactured and Distributed by Metabolic Nutrition, Sunrise, Florida, www.metabolicnutrition.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1047-2014·2014-02-05

    eXtenZone capsules recalled for containing unapproved drug ingredients

    SS Wholesale Inc. is recalling eXtenZone capsules because FDA analysis found undeclared desmethyl carbondenafil and dapoxetine, making the product an unapproved new drug.

    Product
    eXtenZone capsules, 1 capsule per blister pack, Distributed by: P.M.C. Company, Buena Park, CA 90621, UPC 6 89076 49126 6.
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-461-2014·2014-01-22

    Hospira Recalls Aminosyn II Amino Acid Injection Due to Particulate Matter

    Hospira is recalling 17,256 containers of Aminosyn II 10% Amino Acid Injection because a human hair was found in the injection port.

    Product
    Aminosyn II, 10%, Sulfite-Free Amino Acid Injection, 500 mL container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4164-03, UPC (01) 0 030409 416403 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-369-2014·2013-12-25

    Bee Pollen Capsules Recalled for Undeclared Sibutramine

    Zi Xiu Tang Success, LLC is recalling Classic Zi Xiu Tang Bee Pollen Capsules because they contain undeclared sibutramine, an unapproved active ingredient.

    Product
    Classic Zi Xiu Tang, Bee Pollen Capsule, Net Wt. 250 mg x 60 capsules per bottle, Distributed by: Zi Xiu Tang Success, LLC., Trexlertown, PA 18087, UPC 6 937000 700019
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-375-2014·2013-12-25

    Altaire Recalls Carboxymethylcellulose Sodium Eye Drops Due to Non-Sterility

    Altaire Pharmaceuticals is recalling specific lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution because the preservative may not be effective through expiry, posing a non-sterility risk.

    Product
    Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution, 1 FL OZ (30 mL) bottle, sold under the following labels: (a) CVS pharmacy brand LUBRICANT EYE DROPS FOR MILD TO MODERATE DRY EYE, Distributed by CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 053357 7 and UPC 0 50428
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-371-2014·2013-12-25

    Quick Thin capsules recalled for containing unapproved drugs

    Bethel Nutritional Consulting is recalling Quick Thin capsules because FDA analysis detected unapproved drugs sibutramine and phenolphthalein.

    Product
    Quick Thin (citrus aurantium extract, sweet potato fiber, cyamopsis gum powder, alfalfa, mulberry leaf, guarana, spirulina) capsules, 400 mg, 30-count bottle, Distributed by: Bethel, Inc., Tel: (212) 568-5330.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-376-2014·2013-12-25

    Evil Root 1200 mg Recalled for Undeclared Sildenafil

    Fabscout Entertainment, Inc. is recalling Evil Root 1200 mg capsules because the product contains undeclared sildenafil and was marketed without FDA approval.

    Product
    Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd. Address: No. 98, Min zu Road, Lhasa
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-370-2014·2013-12-25

    Zi Xiu Tang Ultimate Formula Recalled for Undeclared Sibutramine

    Zi Xiu Tang Success, LLC is recalling Ultimate Formula capsules because they contain undeclared sibutramine, an ingredient removed from the market for safety reasons.

    Product
    Ultimate Formula, Net Wt. 250 mg, 48 capsules per bottle, Distributed by: Zi Xiu Tang Success, LLC., Trexlertown, PA 18087, UPC 7 9357304140 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-373-2014·2013-12-25

    Purity First B-50 Capsules Recalled for Undeclared Steroids

    Healthy Life Chemistry is recalling B-50 capsules because FDA analysis found undeclared steroids, making the product an unapproved new drug.

    Product
    B-50 capsules, 100-count bottles, labeled in part as Healthy Life Chemistry, By Purity First, Manufactured for: Purity First Health Products, Inc. Healthy Life Chemistry 51 Florida Street, Farmingdale, NY 11735; 1-800-696-7017
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-378-2014·2013-12-25

    PRO POWER MAX Energy Capsules Recalled for Undeclared Sildenafil and Tadalafil

    Fabscout Entertainment is recalling PRO POWER MAX Natural Energy Enhancer capsules because they contain undeclared sildenafil and tadalafil and were marketed without FDA approval.

    Product
    PRO POWER MAX Natural Energy Enhancer, ALL NATURAL HERBS, supplied in 1 capsule per blister pack, Distributed by MSH Distribution LLC
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-380-2014·2013-12-25

    Hospira Recalls Bupivacaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 118,100 vials of 0.25% Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-381-2014·2013-12-25

    Hospira Recalls Bupivacaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 119,600 vials of Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-377-2014·2013-12-25

    Dietary Supplement Recalled for Undeclared Sildenafil and Lack of FDA Approval

    Fabscout Entertainment is recalling 72HP Maximum Potency Male Sexual Enhancement because it contains undeclared sildenafil and was marketed without FDA approval.

    Product
    72HP MAXIMUM POTENCY MALE SEXUAL ENHANCEMENT, Dietary Supplement, supplied in 1 capsule per blister pack, Distributed by: 72HP, Inc. Weston, FL
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-345-2014·2013-12-18

    Volcano Male Enhancement Capsules Recalled for Undeclared Pharmaceutical Ingredients

    Myson Corporation is recalling Volcano Male Enhancement capsules because they contain undeclared active pharmaceutical ingredients, making them unapproved new drugs.

    Product
    Volcano Male Enhancement 1500mg, 1-count capsule packaged in a black round plastic pop top container, (Proprietary Formula, Pueraria lobata, Cinnamon Bark, Cuscuta, Gui, Licorice, Altractylodes, Dang Condonopsis, Dismutase, Cornus, Rubus, Deng Sen Extract, Panax Ginseng, Cordycep
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-220-2014·2013-12-11

    FDA Recalls Compounded Methylprednisolone Vials Linked to Skin Abscesses

    Main Street Family Pharmacy is recalling compounded methylprednisolone vials after seven reports of skin abscesses.

    Product
    Methylprednisolone 80mg/ml (PF) 10ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-210-2014·2013-12-11

    Main Street Compounding Pharmacy Recalls Methylprednisolone Due to Skin Abscess Reports

    Main Street Compounding Pharmacy is recalling methylprednisolone vials after seven reports of skin abscesses potentially linked to the product.

    Product
    Methylprednisolone 100mg/ml, 10ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-021-2014·2013-12-04

    Jack Rabbit Herbal Supplement Recalled for Undeclared Prescription Ingredients

    Jack Rabbit, Inc. is recalling its J.R. Jack Rabbit All Natural Herbal Supplement because FDA testing found undeclared sildenafil and tadalafil.

    Product
    J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack, Order at: www.jackrabbitfourpack.com, Jack Rabbit Inc., 4355 Dow Road, Melbourne, FL 32934
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-929-2013·2013-09-11

    FDA Recalls SexVoltz Herbal Supplement Containing Unapproved Tadalafil

    Beamonstar Products is recalling SexVoltz All Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.

    Product
    SexVoltz All Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 and 12 capsule bottles, Manufactured For: BeaMonstar Products, Queen Creek, AZ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-930-2013·2013-09-11

    Velextra Herbal Supplement Recalled for Containing Unapproved Tadalafil

    Beamonstar Products is recalling Velextra All-Natural Herbal Supplement because it contains tadalafil, an unapproved drug ingredient.

    Product
    Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonstar Products Queen Creek, AZ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-919-2013·2013-09-04

    Rugby Enteric Coated Aspirin 81 mg Recalled for Labeling Error

    Advance Pharmaceutical Inc. is recalling 16,440 bottles of Enteric Coated Aspirin 81 mg due to a label mix-up where one bottle contained Acetaminophen 500 mg.

    Product
    ENTERIC COATED ASPIRIN (NSAID), 81 mg, 120-count tablets per bottle, distributed by: Rugby Laboratories, Inc., Duluth, Georgia 30097, NDC 0536-3086-41, UPC 3 0536-3086-41 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-922-2013·2013-09-04

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    Hospira is recalling 264,432 bags of 0.9% Sodium Chloride Injection because the product may contain fibrous material.

    Product
    0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-920-2013·2013-09-04

    Fresenius Kabi Recalls Magnesium Sulfate Injection Due to Glass Particulates

    Fresenius Kabi is recalling 15,625 vials of Magnesium Sulfate Injection, USP, 50% due to the presence of glass particulate matter.

    Product
    Magnesium Sulfate Injection, USP, 50% (25 grams/50 mL), For IM or IV Use, 50 mL, Single Dose Vial, Rx only, Preservative Free, APP Pharmaceuticals, LLC, Schaumburg, IL, 60173, NDC 63323-064-50
    Category
    Drug
    Distribution
    Distributed nationwide