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

16601–16625 of 17807

LowFDA (Drugs)·D-904-2013·2013-08-28
Novartis Recalls Maalox Antacid Tablets Due to Illegible Packaging Labels
Novartis Consumer Health is recalling Maalox Advanced Maximum Strength Antacid & Antigas chewable tablets because the lot number or expiration date may be illegible on the outer plastic bottle.
Product
Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and simethicone) chewable tablets, 1000 mg/60 mg, Wild Berry flavor, 65-count tablets per bottle, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, NDC 0067-62791-65, UPC 3…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-907-2013·2013-08-28
Novartis Recalls Maalox Antacid Tablets Due to Illegible Labeling
Novartis Consumer Health is recalling Maalox Regular Strength Antacid chewable tablets because the lot number and expiration date may be illegible on the packaging.
Product
Maalox, Regular Strength Antacid (calcium carbonate) chewable tablets, 600 mg, Wintergreen flavor, 50-count tablets per bottle, Novartis Consumer Health Canada Inc., Mississauga, ON L5N 2X7, foreign labeling containing English and French, NPN 02238290, UPC 0 58478 44824 4.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-900-2013·2013-08-28
Stayma Recalls Subpotent Nata Komplete Multi-Vitamin Tablets
Stayma Consulting Service is recalling specific lots of Nata Komplete multi-vitamin tablets because they contain subpotent levels of beta carotene (Vitamin A).
Product
Nata Komplete, containing one 30-count bottle of multi-vitamin tablets (imprinted 909), Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-909-30) and physician samples of nine bottles of 5-multi-vitamin tablets (NDC 76331-909-05 )
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-901-2013·2013-08-28
AbbVie Recalls Mavik Trandolapril Tablets Due to Outdated Package Insert
AbbVie is recalling 704 bottles of Mavik trandolapril tablets 4mg because they were packaged with an outdated version of the package insert.
Product
Mavik¿ trandolapril tablets 4mg, 100 count bottle, Rx only, Manufactured by Halo Pharmaceutical Inc., Whippany, NJ for Abbott Laboratories, North Chicago, IL 60064, USA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-858-2013·2013-08-21
Pallimed Recalls Alprostadil Injection Due to Sterility Assurance Concerns
Pallimed Solutions is recalling 408 vials of Alprostadil IN NS Injection nationwide because FDA inspectional findings raised concerns about sterility assurance.
Product
Alprostadil IN NS Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-884-2013·2013-08-21
Dr. Reddy's Recalls Ranitidine Tablets Due to Microbial Contamination
Dr. Reddy's is recalling specific lots of OTC Ranitidine Hydrochloride tablets because raw material tested positive for Pseudomonas sp.
Product
Ranitidine Hydrochloride Tablets, USP, 150 mg, OTC, a) Equate brand Maximum Strength Acid Reducer, 65 count bottle Dist. By: Wal-Mart Stores, Inc., Bentonville, AR 72710, NDC 49035-404-61 b)Equaline brand maximum strength heartburn relief, , DISTRIBUTED BY SUPERVALU INC., EDEN…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-886-2013·2013-08-21
Sanofi Recalls Subpotent Rifadin Capsules Due to Low Fill
Sanofi-Synthelabo is recalling 998 bottles of Rifadin (rifampin) capsules because some capsules contained less medication than labeled.
Product
Rifadin (rifampin) capsules, USP, 150 mg, 100-count capsules per bottle, Manufactured by: Fabrique par Sanofi-Aventis Canada Inc., Laval, Quebec, Canada H7L4A8, DIN # 02091887
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-857-2013·2013-08-21
Pallimed Acetylcysteine Ophthalmic Solution Recalled for Sterility Concerns
Pallimed Solutions is recalling Acetylcysteine Ophthalmic Solution due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Acetylcysteine Ophthalmic Solution, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-878-2013·2013-08-21
Pallimed Recalls Testosterone Cypionate Injection Due to Sterility Concerns
Pallimed Solutions is recalling 597 vials of compounded Testosterone Cypionate Injection nationwide due to FDA inspectional findings regarding sterility assurance.
Product
Testosterone Cypionate Injection,compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-866-2013·2013-08-21
Pallimed Solutions Recalls Dexamethasone PF Due to Sterility Concerns
Pallimed Solutions is recalling Dexamethasone PF compounded in Woburn, MA, due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Dexamethasone PF, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-876-2013·2013-08-21
Pallimed Solutions Recalls Testosterone Injections Due to Sterility Concerns
Pallimed Solutions is recalling Testosterone Cypionate/Enanthate injections nationwide due to FDA inspectional findings regarding sterility assurance and quality control.
Product
Testosterone Cypionate/Testosterone Enanthate Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-880-2013·2013-08-21
Pallimed Vancomycin Ophthalmic PF Recalled for Sterility Assurance Concerns
Pallimed Solutions is recalling Vancomycin Ophthalmic PF due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Vancomycin Ophthalmic PF, compounded by Pallimed Solutions Pharmacy, Wobrun, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-867-2013·2013-08-21
Pallimed Solutions Recalls DMSO Aqueous Irrigation 50% Due to Sterility Concerns
Pallimed Solutions is recalling DMSO Aqueous Irrigation 50% because FDA inspectional findings raised concerns about quality control procedures that impacted sterility assurance.
Product
DMSO Aqueous Irrigation 50%, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-863-2013·2013-08-21
Pallimed Recalls Cidofovir Ophthalmic Solution Due to Sterility Concerns
Pallimed Solutions is recalling 23 vials of compounded Cidofovir Ophthalmic Solution nationwide due to FDA inspectional findings regarding sterility assurance.
Product
Cidofovir Opthalmic Solution, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-874-2013·2013-08-21
Quadmix Injection Recalled Due to Sterility Assurance Concerns
Pallimed Solutions is recalling Quadmix Injection vials because FDA inspectional findings raised concerns about quality control procedures impacting sterility assurance.
Product
Quadmix Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-868-2013·2013-08-21
Gentamicin Sulfate Irrigation Recalled Due to Sterility Assurance Concerns
Pallimed Solutions is recalling Gentamicin Sulfate Irrigation nationwide because FDA inspections raised concerns about quality control procedures that impacted sterility assurance.
Product
Gentamicin Sulfate Irrigation, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-859-2013·2013-08-21
Pallimed Solutions Recalls Atropine Injection Due to Sterility Concerns
Pallimed Solutions is recalling Atropine Injection compounded in Woburn, MA, due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Atropine Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-860-2013·2013-08-21
Pallimed Solutions Recalls Bacteriostatic Water for Injection Due to Sterility Concerns
Pallimed Solutions is recalling Bacteriostatic Water for Injection because FDA inspections found quality control issues that impacted sterility assurance.
Product
Bacteriostatic Water for Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-864-2013·2013-08-21
Pallimed Recalls Compounded Cyclosporine Ophthalmic Due to Sterility Concerns
Pallimed Solutions is recalling compounded Cyclosporine Ophthalmic because FDA inspections raised concerns about quality control and sterility assurance.
Product
Cyclosporine Ophthalmic, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-875-2013·2013-08-21
Tacrolimus Ophthalmic Recalled Due to Sterility Assurance Concerns
Pallimed Solutions is recalling Tacrolimus Ophthalmic nationwide due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Tacrolimus Ophthalmic, Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-869-2013·2013-08-21
Pallimed Solutions Recalls HCG Vials Due to Sterility Concerns
Pallimed Solutions is recalling 261 vials of compounded HCG Chorionic Gonadotropin nationwide due to FDA inspectional findings regarding sterility assurance.
Product
HCG Chorionic Gonadotropin, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-871-2013·2013-08-21
Pallimed Methylcobalamin Recall Due to Sterility Assurance Concerns
Pallimed Solutions is recalling Methylcobalamin PF vials nationwide due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Methylcobalamin PF, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-870-2013·2013-08-21
Pallimed Solutions Recalls Hydroxyprogesterone Compounded Due to Sterility Concerns
Pallimed Solutions is recalling compounded Hydroxyprogesterone CAPR. (G.S.) due to FDA inspectional findings regarding quality control and sterility assurance.
Product
Hydroxyprogesterone CAPR.(G.S.), compounded by Pallimed Solutions Pharmacy, Woburn MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-865-2013·2013-08-21
Pallimed Recalls Diazepam Injectable Due to Sterility Assurance Concerns
Pallimed Solutions is recalling Diazepam Injectable vials because FDA inspections raised concerns about quality control procedures that impacted sterility assurance.
Product
Diazepam Injectable, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-877-2013·2013-08-21
Pallimed Solutions Recalls Testosterone Injection Due to Sterility Concerns
Pallimed Solutions is recalling Testosterone Cypionate/Propionate Injection nationwide because FDA inspectional findings raised concerns about quality control procedures that impacted sterility assurance.
Product
Testosterone Cypionate/Propionate Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA
Category
Drug
Distribution
Distributed nationwide

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16601–16625 of 17807