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

15051–15075 of 17799

CriticalFDA (Drugs)·D-1333-2014·2014-05-28
Herbal Give Care Recalls Esbelder Fem Supplement for Undeclared Sibutramine
Herbal Give Care Llc is recalling Esbelder Fem Mezcla con L-Carnitina because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Product
Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio,30 capsule bottle, Hecho en Mexico: Soluciones HGC S. de R.L. de C.V. Av. Independencia #1060 Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7502011000251
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1329-2014·2014-05-28
Esbelin Siloutte Mezcal Herbal Recalled for Undeclared Sibutramine
Herbal Give Care Llc is recalling Esbelin Siloutte Mezcal Herbal because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Product
Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio, 30 capsule bottle, Hecho En Mexico Por: Soluciones HGC S. de R.L. de C.V. Av. Independicia #1016 Frac. La Rinconada Aguascalientes, Ags. Mex C.P. 20136, UPC 7502011000060
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1346-2014·2014-05-28
Naturect Capsules Recalled for Undeclared Tadalafil Ingredient
Tendex is recalling Naturect Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.
Product
NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Distributed by P-Boost, Los Angeles, CA 900466
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1332-2014·2014-05-28
Esbelder Man Herbal Blend Recalled for Undeclared Sibutramine
Herbal Give Care Llc is recalling Esbelder Man Herbal Blend because it contains undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Product
Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement, 30 capsule bottle, Made in Mexico: Soluciones S. de R.L. de C.V. Av. Independencia #1060 Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7502011000275
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1339-2014·2014-05-28
ExtenZe 600 mg Recalled for Undeclared Sildenafil and Tadalafil
Schindele Enterprises is recalling ExtenZe 600 mg tablets because they contain undeclared sildenafil or tadalafil, which were marketed without an approved NDA or ANDA.
Product
ExtenZe 600 mg, 30 tablet box, Manufactured for: Biotab Nutraceuticals, Inc., Pasadena, CA.
Category
Drug
Distribution
13 states
CriticalFDA (Drugs)·D-1330-2014·2014-05-28
Herbal Tea Recalled for Undeclared Sibutramine and Related Compounds
Herbal Give Care Llc is recalling Esbelin Siloutte Te herbal tea because it contains undeclared sibutramine and related compounds, making it an unapproved new drug.
Product
Esbelin Siloutte Te, Suplemento Alimenticio, herbal tea in a gold foil/plastic zip-lock pouch. Hecho en Mexico Por: Herbal Give Care, Av Independencia # 1016, Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7562684652553
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1327-2014·2014-05-28
PRO ArthMax Dietary Supplement Recalled for Unapproved Active Ingredients
Human Science Foundation is recalling PRO ArthMax tablets because FDA analysis found unapproved prescription drugs in the product.
Product
PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1326-2014·2014-05-28
Ben Venue Recalls Acetylcysteine Solution Due to Glass Particulate
Ben Venue Laboratories is recalling 5,131 vials of Acetylcysteine Solution, USP, 10% due to the presence of glass particulate matter.
Product
Acetylcysteine Solution, USP, 10%, 30 mL vial, Rx only, Ben Venue Laboratories, Inc., Bedford, OH, NDC 0054-3025-02
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1338-2014·2014-05-28
Magic For Men Recalled for Undeclared Sildenafil and Tadalafil
Schindele Enterprises is recalling Magic For Men dietary supplements because they contain undeclared sildenafil and tadalafil without FDA approval.
Product
Magic For Men, packaged in 1ct blister pack and 12-pill/bottle, 390 mg Manufactured For: BTQ Ski, Inc., Chicago, IL 60638
Category
Drug
Distribution
13 states
CriticalFDA (Drugs)·D-1336-2014·2014-05-28
Dietary Supplement Recalled for Undeclared Sildenafil and Tadalafil Analogs
Schindele Enterprises is recalling Sexy Monkey dietary supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Product
SEXY MONKEY, 2000 mg, 1 count blister, Distributed by A Herbal Bio, Inc., Bayside, NY.
Category
Drug
Distribution
13 states
CriticalFDA (Drugs)·D-1331-2014·2014-05-28
Herbal Give Care Recalls Esbelder Siloutte Supplement for Undeclared Sibutramine
Herbal Give Care is recalling Esbelder Siloutte dietary supplements because they contain undeclared sibutramine, a drug removed from the U.S. market for safety reasons.
Product
Esbelder Siloutte Suplemento Alimenticio, 30 capsule bottle, Hecho en Mexico Por: Herbal Give Care, Av Independencia # 1016, Fracc. La Rinconada, Aguascalientes, Ags. Mex. C.P. 20136. UPC 7502011000268
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1334-2014·2014-05-28
XZONE GOLD Dietary Supplement Recalled for Undeclared Sildenafil and Tadalafil
Schindele Enterprises is recalling XZONE GOLD dietary supplements because they contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Product
XZONE GOLD, 1 capsule blister 750 mg, Distributed by: XZONE, Orlando, FL.
Category
Drug
Distribution
13 states
SevereFDA (Drugs)·D-1341-2014·2014-05-28
Teva Recalls QVAR Inhalation Aerosol Due to Defective Valve
Teva Pharmaceuticals is recalling QVAR inhalation aerosol canisters because the delivery system and valve are defective.
Product
QVAR¿ (beclomethasone dipropionate HFA), 80mcg Inhalation Aerosol, 50 metered inhalations/120 metered inhalations, packaged in an aluminum cylinder, Mktd. by: Teva Respiratory, LLC, Horsham, PA, Mfd. by: 3M Drug Delivery Systems, Northridge, CA.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1343-2014·2014-05-28
Fresenius Recalls phosLo Calcium Acetate GelCaps Due to Cross-Contamination
Fresenius Medical Care is recalling specific lots of phosLo (calcium acetate) GelCaps due to cross-contamination with a tricyclic antidepressant found on the packaging.
Product
phosLo (calcium acetate) GelCaps, 667 mg, 200-count bottle, Rx only, Manufactured for Fresenius Medical Care North America, Waltham, MA 02451, NDC 0781-2081-02
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-1342-2014·2014-05-28
Zydus Recalls Promethazine Hydrochloride Tablets Due to Foreign Tablet Presence
Zydus Pharmaceuticals USA Inc. is recalling 10,200 bottles of Promethazine Hydrochloride 25 mg tablets because atenolol 25 mg tablets were found mixed into the bottles.
Product
PROMETHAZINE HYDROCHLORIDE — PROMETHAZINE HYDROCHLORIDE (PROMETHAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1324-2014·2014-05-28
Teva Recalls Buprenorphine Hydrochloride Sublingual Tablets Due to Impurity Failures
Teva Pharmaceuticals is recalling 17,181 bottles of 2 mg Buprenorphine Hydrochloride Sublingual Tablets because stability testing revealed high out-of-specification impurity levels.
Product
BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 2 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-5378-56, UPC 3 0093-5378-56 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1349-2014·2014-05-28
Red Yeast Rice Supplement Recalled for Excessive Lovastatin Levels
Independent Nutrition Center is recalling Red Yeast Rice High Potency Dietary Supplement because it contains excessive levels of lovastatin, an FDA-approved drug.
Product
Red Yeast Rice High Potency Dietary Supplement, 600 mg, packaged in a) 120-count VegeCaps per bottle (UPC 8 01650 02205 9) and b) 500-count VegeCaps per bottle (UPC 8 01650 02206 6), Manufactured by: Back to Health, Eugene, Oregon 97402.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1337-2014·2014-05-28
MiracleZEN Platinum Recalled for Undeclared Sildenafil and Tadalafil
Schindele Enterprises is recalling MiracleZEN Platinum dietary supplements because they contain undeclared sildenafil and tadalafil, which were marketed without FDA approval.
Product
MiracleZEN Platinum, 1 pill blister pack, 2000 mg capsule, Distributed by: Power Life Distributors, COK Inc., Los Angeles, CA.
Category
Drug
Distribution
13 states
SevereFDA (Drugs)·D-1345-2014·2014-05-28
P-Boost Capsules Recalled for Undeclared Tadalafil Ingredient
Tendex is recalling P-Boost Capsules because FDA analysis found the product contains undeclared tadalafil, making it an unapproved drug.
Product
P-BOOST Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Distributed by P-Boost, Los Angeles, CA 900466
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1344-2014·2014-05-28
SigmaPharm Recalls Liothyronine Sodium Tablets Due to Cross-Contamination
SigmaPharm is recalling four lots of Liothyronine Sodium Tablets 5 mcg due to potential cross-contamination with trace amounts of a previously manufactured product.
Product
LIOTHYRONINE SODIUM — LIOTHYRONINE SODIUM (LIOTHYRONINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1325-2014·2014-05-28
Teva Recalls Buprenorphine Hydrochloride Tablets Due to Impurity Test Failures
Teva Pharmaceuticals is recalling 53,452 bottles of 8 mg Buprenorphine Hydrochloride sublingual tablets because stability testing revealed high out-of-specification impurity levels.
Product
BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 8 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-5379-56, UPC 3 0093-5379-56 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1348-2014·2014-05-28
Forest Pharmaceuticals Recalls Bystolic Tablets for Dissolution Failures
Forest Pharmaceuticals is voluntarily recalling one lot of Bystolic (nebivolol hydrochloride) tablets because dissolution test results failed to meet specifications.
Product
BYSTOLIC — BYSTOLIC (NEBIVOLOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1347-2014·2014-05-28
Oasis Tears Lubricant Eye Drops Recalled for Missing Bottle Labels
Oasis Medical Inc. is recalling 10,549 bottles of Oasis Tears Lubricant Eye Drops because the label on the immediate bottle is missing.
Product
Oasis TEARS, Lubricant Eye Drops, 10mL/0.3 fl. oz. Bottle, OTC Only. Distributed by: OASIS, OASIS Medical, Inc., Glendora, CA 91741. UPC: 8 54819 00002 3.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1322-2014·2014-05-21
REUMOFAN PLUS Tablets Recalled for Undeclared Ingredients and Lack of Approval
Pain Free By Nature is recalling REUMOFAN PLUS tablets because they were marketed without FDA approval and contain undeclared diclofenac and methocarbamol.
Product
REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC. Previene el cancer en los huesos, Nueva presentacion el original.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1318-2014·2014-05-21
FDA Recalls Unapproved Saluta Reduced Glutathione Injection Powder
Flawless Beauty LLC is recalling Saluta (reduced glutathione) Powder for Injection because it was marketed without an approved NDA/ANDA and is labeled for use as an antidote.
Product
Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed by: QAF Pharmaceuticals Inc. Philippines, Unit Unit 202 ECG Building, Multinational Avenue, Multinational Village, Parahaque City, Metro Manila Philippines…
Category
Drug
Distribution
Distributed nationwide

How to read this listing

Filters

15051–15075 of 17799