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 the agency’s own highest classification or reported deaths or serious injuries, 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

15226–15250 of 18042

SevereFDA (Drugs)·D-1389-2014·2014-06-25
John W Hollis Inc Recalls Liver Derivative Complex Injection for Sterility Concerns
John W Hollis Inc is recalling specific lots of Liver Derivative Complex for injection due to a lack of assurance of sterility in the compounded aseptically filled products.
Product
Liver Derivative Complex for injection, each mL contains: Liver Derivative Complex 25.5mg, also contains: Water for Injection, Phenol 0.5%, HCl or NaOH to adjust pH, 10 mL, Compounded by Prescription: JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1397-2014·2014-06-25
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 sterility assurance.
Product
Papaverine HCl 30 mg, Phentolamine Mesylate 1 mg, Alprostadil 20 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-1403-2014·2014-06-25
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 sterility assurance.
Product
Papaverine HCl 30 mg, Phentolamine Mesylate 1 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-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
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
ModerateFDA (Drugs)·D-1383-2014·2014-06-25
Thorne Research Recalls Captomer Capsules Marketed Without FDA Approval
Thorne Research is recalling Captomer capsules because they are marketed as dietary supplements but contain DMSA, an active drug ingredient, making them unapproved new drugs.
Product
Captomer [succinic acid (from 100 mg DMSA)] capsules, 65 mg, 45-count bottles, Manufactured By: Thorne Research, Inc., P.O. Box 25, Dover, Idaho 83825, UPC 6 93749 74002 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1384-2014·2014-06-25
Thorne Research Recalls Captomer-250 Capsules Marketed Without Approval
Thorne Research is recalling Captomer-250 capsules because they are marketed as dietary supplements but contain DMSA, an active drug ingredient, making them unapproved new drugs.
Product
Captomer-250 [succinic acid (from 250 mg DMSA)] capsules, 162 mg, 45-count bottles, Manufactured By: Thorne Research, Inc., P.O. Box 25, Dover, Idaho 83825, UPC 6 93749 73502 1
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1387-2014·2014-06-25
Novartis Recalls Foradil Aerolizer Due to Stability Testing Failures
Novartis is recalling Foradil Aerolizer inhalation powder capsules because they failed stability specifications for particle size distribution.
Product
Foradil Aerolizer (formoterol fumarate inhalation powder), 12 mcg per capsule, 60 Capsules, Rx only, Manufactured for: Merck, Sharpe & Dohne Corp., a subsidiary of Merck & Co., Inc. Whitehouse Station, NJ 08889, Manufactured by: Novartis Pharma AG Basle, Switzerland NDC…
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1371-2014·2014-06-18
Weight Loss Capsules Recalled for Undeclared Phenolphthalein Ingredient
MyNicNaxs, Inc. is recalling REDUCE WEIGHT FRUTA PLANTA Capsules because they contain undeclared phenolphthalein and were marketed without FDA approval.
Product
REDUCE WEIGHT FRUTA PLANTA Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC., Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1378-2014·2014-06-18
Slim Xtreme Weight Loss Capsules Recalled for Undeclared Sibutramine Ingredients
MyNicNaxs, Inc. is recalling Slim Xtreme Weight loss capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine, and were marketed without FDA approval.
Product
Slim Xtreme Weight loss capsules, 500 mg, supplied in 30 count bottles, Another product from Globe All Wellness, LLC Hollywood, FL 33020, 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-1373-2014·2014-06-18
Fruta BIO Capsules Recalled for Undeclared Active Pharmaceutical Ingredients
MyNicNaxs, Inc. is recalling Fruta BIO 400 mg capsules because they contain undeclared sibutramine and phenolphthalein.
Product
Fruta BIO 400 mg capsules, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1375-2014·2014-06-18
FDA Recalls Unapproved Weight Loss Pills Containing Undeclared Phenolphthalein
MyNicKnaxs is recalling weight reduction pills marketed without FDA approval because they contain undeclared phenolphthalein.
Product
Pill for weight reduction, (Japanese Chinese Formula from Japan Hokkaido Cangye Pharmacy Co, Ltd) 400 mg, supplied in 40 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
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-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-1370-2014·2014-06-18
Bella Vi AMP'D UP Weight Loss Supplement Recalled for Undeclared Drugs
Pure Edge Nutrition is recalling Bella Vi AMP'D UP weight loss capsules because they contain undeclared sibutramine and phenolphthalein.
Product
Bella Vi AMP'D UP Advanced Weight Loss 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-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-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-1362-2014·2014-06-18
Pharmakon Recalls Midazolam Syringes Containing Twice Stated Dosage
Pharmakon Pharmaceuticals is recalling specific lots of Midazolam syringes because they contain twice the stated amount of the drug.
Product
Midazolam 0.2 mg/2 mL 0.9% Sodium Chloride syringes, Total dosage: 0.4 mg per 2 mL, Rx Only, Pharmakon Pharmaceuticals, Inc., 14450 Getz Rd, Noblesville, Indiana, NDC 45183-0014-69.
Category
Drug
Distribution
1 state
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-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-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-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-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

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15226–15250 of 18042