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

11976–12000 of 18028

ModerateFDA (Drugs)·D-1357-2016·2016-07-20
FDA Recalls Te Xiao BaiNeiTing Herbal Supplement for Unapproved Drug Claims
Murray International Trading Co. is recalling 17 boxes of Te Xiao BaiNeiTing Herbal Supplement because the product is marketed with drug claims without an approved NDA or ANDA.
Product
Te Xiao BaiNeiTing Herbal Supplement (Naphazoline HCl Solution 0.1%) liquid, Net Wt. 15ml, packaged in a bottle within a box, Produced by: Good Harvests (Asia) Trading Co., Ltd, Imported by Murray Int'l Trading Co., Inc. New York, NY 10013, UPC 7 67533 86115 6, remaining…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1354-2016·2016-07-20
Wupooser Kai Yeung Pill Recalled for Unapproved Drug Claims
Murray International Trading Co. is recalling Wupooser Kai Yeung Pill because it is marketed with drug claims without FDA approval.
Product
WUPOOSER KAI YEUNG PILL, packaged in a bottle within a box, Made in The Peoples Republic of China, remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1350-2016·2016-07-20
Murray International Recalls Tien Ma Tou Tong Wan Pills for Unapproved Drug Claims
Murray International Trading Co. is recalling Tien Ma Tou Tong Wan pills because they bear drug claims despite being marketed as dietary supplements.
Product
Tien Ma Tou Tong Wan (Condensed pills), packaged in 100-count bottles within a box, Kwangchow First Chinese Medicine Factory, Kwangchow, China; remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1356-2016·2016-07-20
Ping On Ointment Recalled for Unapproved Drug Claims
Murray International Trading Co. is recalling Ping On Ointment because it is marketed as a dietary supplement but bears drug claims, making it an unapproved drug.
Product
PING ON OINTMENT RELIEF FOR MUSCULAR PAIN, packaged in a packet of 12-count 8gm containers within a box, PING ON OINTMENT CO LTD, PING ON OINTMENT INTERNATIONAL LTD, 149 Queen's Road West, Hong Kong, UPC 8 33679 00001 5, remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1436-2016·2016-07-20
Apotex Recalls Duloxetine Capsules Due to Dissolution Failure
Apotex Scientific is recalling Duloxetine Delayed-Release Capsules, 60 mg, because stability testing revealed out-of-specification dissolution results.
Product
Duloxetine Delayed-Release Capsules, USP, 60 mg, 30-count bottles, Rx only, Manufactured by Apotex Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2997-3; UPC # 360505299737;
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1440-2016·2016-07-20
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling specific lots of Daytrana transdermal patches because the release liner may be difficult to remove.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1355-2016·2016-07-20
Murray International Trading Recalls Farser Kai Yeung Pill for Unapproved Drug Claims
Murray International Trading Co., Inc. is recalling Farser Kai Yeung Pill because it is marketed with drug claims without FDA approval.
Product
FARSER KAI YEUNG PILL, packaged in a bottle within a box, Made in The Peoples Republic of China, remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1345-2016·2016-07-20
Murray International Recalls Unapproved Facial Pigmentation Pills
Murray International Trading Co. is recalling 84 bottles of facial pigmentation pills marketed without FDA approval. The products bear drug claims but are labeled as dietary supplements.
Product
PATCH-REMOUING PILL (For Facial Pigmentation), packaged in a bottle within a box, Kwang Chow Pharm. Ind. Corp., remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1352-2016·2016-07-20
Peking Niu-Huang Chieh-Tu-Pien Tablets Recalled for Unapproved Drug Claims
Murray International Trading Co. is recalling Peking Niu-Huang Chieh-Tu-Pien Tablets because they bear drug claims without FDA approval.
Product
PEKING NIU-HUANG CHIEH-TU-PIEN Tablets (Sugar Coated), packaged in 50-count bottles within a box, BEIJING TUNG JEN TANG. BEIJING CHINA; remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1236-2016·2016-07-20
Medaus Recalls Pyridoxine HCL Vials Due to Sterility Concerns
Medaus, Inc. is recalling Pyridoxine HCL 100mg/mL vials because the company cannot ensure the product is sterile.
Product
PYRIDOXINE HCL 100MG/ML W/PRES (BENZYL ETOH 0.02%), 5ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1358-2016·2016-07-20
Murray International Recalls Unapproved Flucinonide Ointment Cream
Murray International Trading Co., Inc. is recalling 97 boxes of FUQINGSONG RELIEF CREAM because it is marketed as a dietary supplement but bears drug claims, making it an unapproved drug.
Product
FUQINGSONG RELIEF CREAM (Flucinonide Ointment), packaged in 50-count individually labeled pieces Net Wt. 0.32oz (10g) within a box, MANUFACTURED BY: TIANJIN MAEDICAL & PHARMACEUTICAL CO., LTD. ADDREST: 96 BAWAEI ROAD, HEDONG COUNTY, TIANJIN CITY, remaining labeling contains…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1353-2016·2016-07-20
Gastrodia Capsules Recalled for Unapproved Drug Claims
Murray International Trading Co. is recalling Gastrodia Capsules because they are marketed as dietary supplements but contain drug claims, making them unapproved drugs.
Product
GASTRODIA CAPSULES, packaged in 30-count bottles within a box, LANZHOU MANUFACTORY OF CHINA. GANSU CHINA; remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1346-2016·2016-07-20
ChingChunBao Anti-Aging Tablets Recalled for Unapproved Drug Claims
Murray International Trading Co. is recalling ChingChunBao Anti-Aging Tablets because they bear drug claims without an approved NDA or ANDA.
Product
ChingChunBao ANTI-AGING TABLETS, packaged in 80-count bottles within a box, UPC 0 49987 01144 9, remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1438-2016·2016-07-20
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling 7,850 boxes of Daytrana (methylphenidate) transdermal patches because the release liner may be difficult to remove.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1439-2016·2016-07-20
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling 2,088 boxes of Daytrana transdermal patches because the release liner may be difficult to remove.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1437-2016·2016-07-20
Apotex Recalls Duloxetine Capsules Due to Dissolution Failure
Apotex Scientific is recalling Duloxetine Delayed-Release Capsules because stability testing revealed out-of-specification dissolution results.
Product
Duloxetine Delayed-Release Capsules, USP, 30 mg, 30-count bottles, Rx only, Manufactured by Apotex Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2996-3; UPC # 360505299638.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1255-2016·2016-07-20
Golden State Medical Supply Recalls Duloxetine Capsules Due to Labeling Error
Golden State Medical Supply is recalling 2,077 bottles of Duloxetine 60 mg capsules because the container labels display an incorrect expiration date.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1435-2016·2016-07-20
Apotex Recalls Duloxetine Capsules Due to Failed Dissolution Testing
Apotex Scientific is recalling specific lots of Duloxetine Delayed-Release Capsules because they failed dissolution specifications during stability testing.
Product
Duloxetine Delayed-Release Capsules, USP, 20 mg, 60-count bottles, Rx only, Manufactured by Apotex Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2995-6; UPC # 360505299560;
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1441-2016·2016-07-20
West-Ward Recalls Oxycodone Hydrochloride Oral Solution for Impurity Failures
West-Ward Columbus Inc. is recalling 1,182 bottles of Oxycodone Hydrochloride Oral Solution due to failed impurities and degradation specifications.
Product
OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1149-2016·2016-07-13
XCEL Capsules Recalled for Undeclared Fluoxetine and Phenolphthalein
Bee Extremely Amazed LLC is recalling XCEL Capsules marketed as a dietary supplement because they contain undeclared fluoxetine and phenolphthalein.
Product
XCEL Capsules, 300 mg, 60-count bottles, Manufactured for JNS Health
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1145-2016·2016-07-13
Prime Capsules Recalled for Undeclared Sibutramine and Phenolphthalein
Bee Extremely Amazed LLC is recalling Prime Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.
Product
Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St. #392 Columbus, IN 47203
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1144-2016·2016-07-13
Oasis Capsules Recalled for Undeclared Sibutramine and Phenolphthalein
Bee Extremely Amazed LLC is recalling Oasis Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.
Product
Oasis Capsules, 500mg, 45-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando FL 32801 (407)930-4043
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1151-2016·2016-07-13
ZI XIU TANG Beauty Capsules Recalled for Undeclared Sibutramine
Bee Extremely Amazed LLC is recalling ZI XIU TANG Beauty Face & Figure Capsules because they contain undeclared sibutramine, a withdrawn drug.
Product
ZI XIU TANG BEAUTY FACE & FIGURE Capsules, 250 mg, 60-count bottles
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1143-2016·2016-07-13
La' Trim Plus Capsules Recalled for Undeclared Withdrawn Ingredients
Bee Extremely Amazed LLC is recalling La' Trim Plus Capsules because the product contains undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.
Product
La' Trim Plus Capsules, 350 mg, 60-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando, FL 32801 (407) 930-4043
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1137-2016·2016-07-13
Hospira Recalls Magnesium Sulfate Injection Due to Particulate Matter
Hospira Inc. is recalling specific lots of Magnesium Sulfate Injection due to confirmed particulate matter. The recall covers 88,500 vials distributed in the US and several Middle Eastern countries.
Product
Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.
Category
Drug
Distribution
Distributed nationwide

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11976–12000 of 18028