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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

10076–10100 of 11860

SevereFDA (Drugs)·D-1396-2014·2014-06-25
John W Hollis Inc Recalls Methylcobalamin Injectable Due to Sterility Concerns
John W Hollis Inc is recalling Methylcobalamin 1000 mcg injectable products because they lack assurance of sterility. The recall covers Lot # 1862 distributed nationwide.
Product
METHYLCOBALAMIN FOR INTRAMUSCULAR OR SUBCUTANEOUS USE ONLY, Methylcobalamin 1000 mcg, Also Contains: Benzyl Alcohol, Sodium Chloride, Water, Hydrochloric Acid, and/or Sodium Hydroxide, 30 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1391-2014·2014-06-25
John W Hollis Recalls Polidocanol 5% Injection Due to Sterility Concerns
John W Hollis Inc is recalling Polidocanol 5% Solution for Injection because the company cannot ensure the product is sterile.
Product
Polidocanol 5% Solution for Injection, each mL contains Polidocanol (Laureth 9) 50 mg, also contains Sterile Water for Injection, Ethyl Alcohol, Anhydrous Chlorobutanol, 50 mL Vial, JOHN HOLLIS Pharmacist Inc, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1392-2014·2014-06-25
John W Hollis Inc Recalls Testosterone Cypionate Injection Due to Sterility Concerns
John W Hollis Inc is recalling specific lots of Testosterone Cypionate for Injection because the products lack assurance of sterility.
Product
Testosterone Cypionate for Injection, each mL contains Testosterone Cypionate 200 mg, also contains: Cotton Seed Oil, Benzyl Benzoate, Benzyl Alcohol, Rx Only, 10 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1388-2014·2014-06-25
John W Hollis Recalls Polidocanol Injection Due to Sterility Concerns
John W Hollis Inc is recalling Polidocanol 0.5% Solution for Injection because the products lack assurance of sterility.
Product
Polidocanol 0.5% Solution for Injection, Polidocanol (Laureth 9) 5mg, 50 mL, JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1406-2014·2014-06-25
John W Hollis Recalls Polidocanol 1% Injection Due to Sterility Concerns
John W Hollis Inc. is recalling Lot 2868 of Polidocanol 1% Solution for Injection because the company cannot ensure the product is sterile.
Product
Polidocanol 1% Solution for Injection, each mL contains Polidocanol (Laureth 9) 10 mg, also contains Sterile Water for Injection, Ethyl Alcohol, Anhydrous Chlorobutanol, 50 mL, JOHN HOLLIS Pharmacist, Inc. 110 B2 Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1386-2014·2014-06-25
Actavis Recalls Subpotent Vancomycin Hydrochloride Capsules Nationwide
Actavis Inc is recalling 6,913 packages of Vancomycin Hydrochloride Capsules because the drug is subpotent. The recall covers distribution across the United States.
Product
Vancomycin Hydrochloride Capsules, USP, 250 mg. 20 Capsules on 2 x 10 Capsule Blister Cards, Rx Only. Mfd. for: Watson Pharma Inc., Parsippany, NJ 07054 USA. Mfd. by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237 USA. NDC 0591-3561-15.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1405-2014·2014-06-25
John W Hollis Inc Recalls Pyridoxine HCl Injectable Due to Sterility Concerns
John W Hollis Inc is recalling Pyridoxine HCl 100mg injectable products because they lack assurance of sterility. Consumers should stop using the product and contact their pharmacist.
Product
PYRIDOXINE HCL, Pyridoxine HCl 100mg, Also Contans: Benzyl Alcohol, Sodium Chloride, Water, Hydrochloric Acid, and/or Sodium Hydroxide, 30 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1399-2014·2014-06-25
John W Hollis Inc Recalls Compounded Injectable Products Due to Sterility Concerns
John W Hollis Inc is recalling specific lots of compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.
Product
Papaverine HCl 30 mg, Phentolamine Mesylate 2 mg, Alprostadil 40 mcg, a) 5 mL and b) 10 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1395-2014·2014-06-25
John W Hollis Recalls Levocarnitine Injection Due to Sterility Concerns
John W Hollis Inc. is recalling Levocarnitine Solution for injection because the company cannot ensure the product is sterile. The recall covers specific lots distributed nationwide.
Product
Levocarnitine Solution for injection, l-Carnitine 50 mg, Also Contains Sterile Water for Injection and Benzyl Alcohol pH adjusted with HCl, 50 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1402-2014·2014-06-25
John W Hollis Inc Recalls Compounded Injectable Products Due to Sterility Concerns
John W Hollis Inc is recalling compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of assurance of sterility.
Product
Papaverine HCl 30 mg, Phentolamine Mesylate 0.5 mg, Alprostadil 10 mcg, a) 5 mL and b) 10 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1390-2014·2014-06-25
John W Hollis Inc Recalls Cyanocobalamin Injection Due to Sterility Concerns
John W Hollis Inc is recalling specific lots of Cyanocobalamin injection because the products lack assurance of sterility. The recall covers 2,650 mL distributed nationwide.
Product
CYANOCOBALAMIN FOR INTRAMUSCULAR OR SUBCUTANEOUS USE ONLY, Each mL contains: Cyanocobalamin 1000 mcg, , Also Contains: Benzyl Alcohol, Sodium Chloride, Water, Hydrochloric Acid, and/or Sodium Hydroxide, 30 mL, JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203, 6
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1393-2014·2014-06-25
John W Hollis Inc Recalls MIC Plus B12 Injectable Due to Sterility Concerns
John W Hollis Inc is recalling MIC Plus B12 injectable vials because the products lack assurance of sterility. Consumers should stop using the affected lots immediately.
Product
MIC PLUS B12, Adenosine, L-Carnitine, Contains: Methionine 15mg, Choline 100mg, Inositol 50mg, B 12, 0.200mg, Adenosine 20mg, L-Carnitine 30mg/ML, 30ML MULTI DOSE VIAL, BENZYL ALCOHOL AS A PRESERVATIVE, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-32
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1385-2014·2014-06-25
Ferring Recalls TEV-TROPIN Injection Due to Potential Silicone Oil Contamination
Ferring Pharmaceuticals is recalling TEV-TROPIN injection bottles due to potential silicone oil contamination from a leaking line during manufacturing.
Product
TEV-TROPIN [somatropin (rDNA origin) for injection] 5 mg (15 IU) 1-count bottle, Rx Only, Manufactured in Israel, Distributed by: Gate Pharmaceuticals div. of Teva Pharmaceuticals USA Sellersville,PA 18960. NDC 57844-713-46
Category
Drug
Distribution
1 state
CriticalFDA (Drugs)·D-1380-2014·2014-06-18
Meizitang Botanical Slimming Capsules Recalled for Undeclared Sibutramine Ingredients
MyNicNaxs, Inc. is recalling Meizitang Strong Version Botanical Slimming capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine.
Product
Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1367-2014·2014-06-18
Bella Vi BTrim Ultimate Boost Recalled for Undeclared Dangerous Ingredients
Pure Edge Nutrition is recalling Bella Vi BTrim Ultimate Boost capsules because they contain undeclared sibutramine and phenolphthalein.
Product
Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules, 30 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1361-2014·2014-06-18
Greenstone Recalls Venlafaxine Capsules Due to Foreign Capsule Contamination
Greenstone LLC is recalling 16,018 bottles of Venlafaxine HCl Extended-Release Capsules because a foreign capsule was found in a bottle from the same packaging campaign.
Product
Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0182-2, UPC 3 59762-0182-2 9.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1376-2014·2014-06-18
SlimEasy Herbs Capsules Recalled for Undeclared Sibutramine
MyNicNaxs, Inc. is recalling SlimEasy Herbs Capsules because they contain undeclared sibutramine and N-desmethylsibutramine and were marketed without an approved NDA/ANDA.
Product
SlimEasy Herbs Capsule, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1379-2014·2014-06-18
Magic Slim capsules recalled for undeclared pharmaceutical ingredients
MyNicNaxs, Inc. is recalling Magic Slim capsules because they contain undeclared active pharmaceutical ingredients and were marketed without an approved NDA or ANDA.
Product
Magic Slim capsules, supplied in 60 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1366-2014·2014-06-18
Bella Vi BTrim MAX Recalled for Undeclared Sibutramine and Phenolphthalein
Pure Edge Nutrition is recalling Bella Vi BTrim MAX dietary supplements because they contain undeclared sibutramine and phenolphthalein and were marketed without FDA approval.
Product
Bella Vi BTrim MAX Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1364-2014·2014-06-18
vitaliKOR Dietary Supplement Recalled for Undeclared Prescription Ingredients
Vitality Research Labs is recalling vitaliKOR capsules because FDA sampling found undeclared vardenafil and tadalafil. The product was marketed without an approved NDA or ANDA.
Product
vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1368-2014·2014-06-18
Bella Vi eXtreme ACCELERATOR Recalled for Undeclared Sibutramine and Phenolphthalein
Pure Edge Nutrition is recalling Bella Vi eXtreme ACCELERATOR capsules because they contain undeclared sibutramine and phenolphthalein.
Product
Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules, 30 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1377-2014·2014-06-18
Meizi Evolution Soft Gel Capsules Recalled for Undeclared Active Ingredients
MyNicNaxs, Inc. is recalling Meizi Evolution Soft Gel Capsules because the product was marketed without an approved NDA/ANDA and contains undeclared active pharmaceutical ingredients.
Product
Meizi Evolution Soft Gel Capsules, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1374-2014·2014-06-18
FDA Recalls Super Fat Burning Bomb Capsules for Undeclared Ingredients
MyNicNaxs, Inc. is recalling Super Fat Burning Bomb Capsules because they contain undeclared active pharmaceutical ingredients, phenolphthalein and N-desmethylsibutramine.
Product
Super Fat Burning Bomb Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1372-2014·2014-06-18
Jianfeijindan Activity Girl Capsules Recalled for Undeclared Sibutramine Analog
MyNicNaxs, Inc. is recalling Jianfeijindan Activity Girl Capsules because they contain an undeclared sibutramine analog and were marketed without FDA approval.
Product
JIANFEIJINDAN Activity Girl Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1369-2014·2014-06-18
Bella Vi INSANE AMP'D Dietary Supplement Recalled for Undeclared Ingredients
Pure Edge Nutrition is recalling Bella Vi INSANE AMP'D dietary supplements because they contain undeclared sibutramine and phenolphthalein.
Product
Bella Vi INSANE AMP'D Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
Category
Drug
Distribution
Distributed nationwide

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10076–10100 of 11860