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

9751–9775 of 17987

SevereFDA (Drugs)·D-0656-2018·2018-04-25
Partell Specialty Pharmacy Recalls MVI-7 Injectable Due to Sterility Concerns
Partell Specialty Pharmacy is recalling MVI-7 injectable vials because a non-approved sterilization method was used, raising concerns about product sterility.
Product
MVI-7 (B1-100mg/B3-100mg, B5-252 mg, B6-102mg, Vit C-2500 mg, B12-10mg, Mag-1000 mg)/ vial liquid injectable, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0684-2018·2018-04-25
Lupin Recalls Cefdinir Powder for Oral Suspension Due to Superpotency
Lupin Pharmaceuticals is voluntarily recalling 40,824 bottles of Cefdinir powder for oral suspension because the drug was found to be superpotent.
Product
CEFDINIR — CEFDINIR (CEFDINIR)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0671-2018·2018-04-25
Partell Specialty Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Testosterone/Anastrozole pellets because a non-approved sterilization method was used, raising concerns about sterility assurance.
Product
Testosterone/Anastrozole 60 mg/1 mg pellets packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0638-2018·2018-04-25
Partell Specialty Pharmacy Recalls Glutathione Vials Due to Sterility Concerns
Partell Specialty Pharmacy is recalling four vials of Glutathione 200mg/mL in Nevada because the products were sterilized using a non-approved method.
Product
Glutathione 200mg/mL, 10mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0639-2018·2018-04-25
Partell Specialty Pharmacy Recalls HCG Vials Due to Sterility Concerns
Partell Specialty Pharmacy is recalling HCG 1000 units/mL vials in Nevada because a non-approved sterilization method was used.
Product
HCG 1000 units/mL, packaged in a) 2 mL and b) 6 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0660-2018·2018-04-25
Partell Specialty Pharmacy Recalls TM Drug Vials Due to Sterility Concerns
Partell Specialty Pharmacy is recalling specific lots of TM drug vials because they were sterilized using a non-approved method.
Product
TM (ALP 50/PAPAV 30/PHENT1.5 mg), 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0674-2018·2018-04-25
Partell Specialty Pharmacy Recalls Estradiol Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Estradiol 12.5 mg pellets in Nevada due to a non-approved sterilization method.
Product
Estradiol 12.5 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0658-2018·2018-04-25
Partell Specialty Pharmacy Recalls TM #4 Due to Sterility Concerns
Partell Specialty Pharmacy is recalling TM #4 drug products because a non-approved method of sterilization was used.
Product
TM #4 (ALP 20/PAPAV/PHENT 2), 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0668-2018·2018-04-25
Partell Specialty Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Testosterone 55 mg pellets in Nevada because they were sterilized using a non-approved method.
Product
Testosterone 55 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0667-2018·2018-04-25
Partell Specialty Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Testosterone 50 mg pellets because they were sterilized using a non-approved method.
Product
Testosterone 50 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
HighFDA (Drugs)·D-0641-2018·2018-04-25
Partell Specialty Pharmacy Recalls Methionine, Inositol, and Choline Vials
Partell Specialty Pharmacy is recalling 11 vials of Methionine/Inositol/Choline in Nevada due to a non-approved sterilization method.
Product
Methionine15mg/Inositol 50mg/Choline 100mg, packaged in a) 5mL and b) 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
HighFDA (Drugs)·D-0673-2018·2018-04-25
Partell Specialty Pharmacy Recalls Estradiol Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Estradiol 10 mg pellets in Nevada due to a non-approved sterilization method.
Product
Estradiol 10 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
Category
Drug
Distribution
1 state
HighFDA (Drugs)·D-0664-2018·2018-04-25
Partell Specialty Pharmacy Recalls Testosterone Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Testosterone 25 mg pellets because they were sterilized using a non-approved method.
Product
Testosterone 25 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
Category
Drug
Distribution
1 state
HighFDA (Drugs)·D-0679-2018·2018-04-25
Partell Specialty Pharmacy Recalls Estradiol Pellets Due to Sterility Concerns
Partell Specialty Pharmacy is recalling Estradiol 40 mg pellets in Nevada due to a non-approved sterilization method.
Product
Estradiol 40 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0630-2018·2018-04-25
WipeEssentials Wet Wipes Recalled for Poor Quality Water
Diamond Wipes International is recalling WipeEssentials Wet Wipes because they were manufactured with poor quality water.
Product
WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA 91710, UPC 7 66670 03988 6.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0633-2018·2018-04-25
AvKARE Recalls Amantadine HCl Capsules for Dissolution Failure
AvKARE Inc. is recalling 2,135 cartons of Amantadine HCl Capsules, 100 mg, because the product failed dissolution specifications.
Product
AMANTADINE HCL — AMANTADINE HCL (AMANTADINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0627-2018·2018-04-25
Noven Recalls Daytrana Methylphenidate Patches Due to Adhesive Defect
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the adhesive transfer is out of specification.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0696-2018·2018-04-25
Fluconazole Injection Recalled Due to Labeling Mix-Up
Renaissance Lakewood, LLC is recalling Fluconazole Injection due to a labeling mix-up where a 50 mL bag was found in a 100 mL package.
Product
Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), package in 100 mL bags, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902, By: Claris Injectables Limited, Sarkhei-Bavla Road, Chacharwadi-Vasna, Ahmedabad, I
Category
Drug
Distribution
0 states
ModerateFDA (Drugs)·D-0629-2018·2018-04-25
ACURE Clarifying Acne Towelettes Recalled for Poor Quality Water
Diamond Wipes International is recalling ACURE clarifying acne towelettes because they were manufactured with poor quality water.
Product
ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0683-2018·2018-04-25
Leadiant Recalls Subpotent Cystaran Ophthalmic Solution
Leadiant Biosciences is recalling 3,398 bottles of Cystaran ophthalmic solution because the active ingredient was below the required specification.
Product
CYSTARAN — CYSTARAN (CYSTEAMINE HYDROCHLORIDE)
Category
Drug
Distribution
0 states
ModerateFDA (Drugs)·D-0631-2018·2018-04-25
Sandoz Recalls Triamterene and Hydrochlorothiazide Tablets Due to Cross-Contamination
Sandoz Incorporated is recalling specific lots of Triamterene and Hydrochlorothiazide Tablets due to the presence of unrelated ingredients.
Product
Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0632-2018·2018-04-25
Pharmedium Recalls Vasopressin Injection Due to Manufacturing Deviations
Pharmedium Services, LLC voluntarily recalled 72 bags of Vasopressin Injection due to cGMP deviations. The product was distributed in Massachusetts and Washington.
Product
Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL), Rx only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0623-2018·2018-04-18
Elroselabs Recalls Conzerol Hydrogen Peroxide Gel Due to cGMP Deviations
Elroselabs Inc. is voluntarily recalling Conzerol Hydrogen Peroxide Gel 3% nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Product
Conzerol (antipoxin) H2O2 Gel, Hydrogen Peroxide Gel 3%, 1.5 oz. tube, OTC, Manufactured for Elrose Labs, Inc., Sanford, FL
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0621-2018·2018-04-18
Elroselabs Recalls Conzerol Topical Cream Due to Manufacturing Deviations
Elroselabs Inc. is voluntarily recalling Conzerol topical cream nationwide due to cGMP deviations. The recall was initiated in March 2018 and terminated in December 2020.
Product
Conzerol zero molluscum contagiosum, Topical Cream, Net weight 0.78 (22g), Elrose Labs, Sanford Fl 32771 USA --- NDC 70223-001-06
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0624-2018·2018-04-18
FDA Recalls Zhong Hua Jiu Menthol Patches for GMP Deviations
United Pacific Co Ltd is recalling Zhong Hua Jiu (menthol 1%) Patches because they were produced with substandard GMP manufacturing processes.
Product
Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02
Category
Drug
Distribution
Distributed nationwide

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9751–9775 of 17987