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

17676–17700 of 18050

LowFDA (Drugs)·D-042-2013·2012-11-14
Valeant Recalls Subpotent AcneFree 24 Hour Clearing System
Valeant Pharmaceuticals is recalling AcneFree 24 Hour Clearing System cartons because the benzoyl peroxide active ingredient is subpotent and the labels contain errors regarding inactive ingredients.
Product
AcneFree 24 Hour Clearing System containing 1-count 4 fl oz (118 mL) Oil-Free Purifying Cleanser (benzoyl peroxide 2.5% w/v) AFCS-0101-00, 1-count 4 fl oz (118 mL) Renewing Toner AFCS-0201-01, and 1-count 2 fl oz (59 mL) Repair Lotion (benzoyl peroxide 3.7% w/v) AFCS-0301-00 per…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-048-2013·2012-11-14
FDA Recalls Subpotent AcneFree Benzoyl Peroxide Cleanser
Valeant Pharmaceuticals is recalling AcneFree Severe Maximum Strength Acne Pore Cleanser because the benzoyl peroxide ingredient is subpotent and the label contains errors.
Product
AcneFree Severe Maximum Strength Acne Pore Cleanser (benzoyl peroxide 5% w/v), 3 oz (85 g) canister, Dist. by: University Medical Pharmaceuticals Corp., Irvine, CA 92618, UPC 7 88521 13350 9.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-047-2013·2012-11-14
Valeant Recalls Subpotent AcneFree 3-in-1 Acne Night Repair Foam
Valeant Pharmaceuticals is recalling AcneFree 3-in-1 Acne Night Repair Foam because the salicylic acid ingredient is subpotent and the label is inaccurate.
Product
AcneFree 3-in-1 Acne Night Repair Foam (retinol + salicylic acid 1.5% w/v), 3 oz (85 g) canister, Dist. by: University Medical Pharmaceuticals Corp., Irvine, CA 92618, UPC 7 88521 13548 6.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-038-2013·2012-11-07
FDA Recalls Unapproved X-Rock 3 Day Pill For Men
Coral Rock Man, Inc. is recalling X-Rock 3 Day Pill For Men because the product was marketed without an approved NDA/ANDA and tested positive for Sildenafil and analogs.
Product
X-ROCK 3 Day Pill For Men, supplied in 1 and 2 capsule blister packs and 6, 12 and 24 count bottles, UPC 0 00309 50792 7, Distributed by: MATE Enterprises, Miami, Florida 33139, Some labeled as: Manufactured by CRM Laboratories, Distributed by XRock Industries, Ft. Lauderdale…
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-039-2013·2012-11-07
Z-ROCK Male Supplement Recalled for Unapproved Sildenafil Content
Coral Rock Man, Inc. is recalling Z-ROCK All Natural Male Supplement because testing revealed the presence of Sildenafil and its analogs, which were not approved in the product.
Product
Z-ROCK All Natural Male Supplement. 1 capsule blister pack, UPC 0 00309 50792 7, Distributed by Zrock USA PO Box 668297, Pompano Beach, FL 33066
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-037-2013·2012-11-07
X-ROCK For Men Recalled for Unapproved Prescription Drug Ingredients
XRock Industries is recalling X-ROCK For Men dietary supplements because testing revealed the presence of unapproved prescription drug ingredients.
Product
X-ROCK For Men, Dietary Supplement, Manufactured by CRM Laboratories, Distributed by XRock Industries, PO Box 120863, Ft. Lauderdale, FL 33312, 0 00309 50792 7. UPC on labeling is: 0 00309 50792 7. UPC in Press Release is: 0030950792.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-035-2013·2012-11-07
Target UP & UP Kids Foaming Hand Sanitizer Recalled for Microbial Contamination
DermaCare is recalling 43,272 bottles of UP & UP brand kids' foaming hand sanitizer due to high microbial counts.
Product
UP & UP brand, kid's foaming hand sanitizer, alcohol free, 99.9% effective against germs, Sweet s'melon, 6.7FL oz (200mL), Distributed by Target Corp., Minneapollis, MN 55403
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-034-2013·2012-11-07
Target UP & UP Kids Foaming Hand Sanitizer Recalled for Microbial Contamination
DermaCare is recalling UP & UP brand kids' foaming hand sanitizer sold at Target due to laboratory findings of high total plate count above specification.
Product
UP & UP brand, kid's foaming hand sanitizer, alcohol free, 99.9% effective against germs, Apple-cleani, 6.7FL oz (200mL), Distributed by Target Corp., Minneapollis, MN 55403
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-036-2013·2012-11-07
Ben Venue Recalls Leucovorin Calcium Injection Due to Particulate Matter
Ben Venue Laboratories is recalling 226,010 vials of Leucovorin Calcium Injection due to the presence of visible crystalline particulates.
Product
Leucovorin Calcium Injection USP, single use vials, 10mg/mL; 50mL, Rx only, Manufactured by: Ben Venue Labs, Inc., Bedford, OH 44146, NDC# 55390-009-01(Bedford); NDC# 55390-826-01(Novaplus)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-020-2013·2012-10-31
Hospira Recalls Overfilled Hydromorphone Hydrochloride Injection Cartridges
Hospira is recalling 216,880 units of Hydromorphone Hydrochloride Injection because the prefilled cartridges were found to be overfilled, containing more than the labeled 1 mL volume.
Product
HYDROMORPHONE HYDROCHLORIDE — HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-031-2013·2012-10-31
Raritan Pharmaceuticals Recalls Premier Value Fiber Plus Calcium Capsules
Raritan Pharmaceuticals is recalling Premier Value Fiber Plus Calcium Supplement Capsules due to possible C. difficile contamination in raw materials.
Product
Premier Value Fiber Plus Calcium Supplement Capsules, 120 capsules per bottle, Distributed by: Chain Drug Consortium, LLC, Boca Raton, FL, UPC 8-40986-01987-6
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-012-2013·2012-10-31
Bristol-Myers Squibb Recalls BiCNU Injection Kits Due to Overfilled Vials
Bristol-Myers Squibb is recalling 31,481 BiCNU kits nationwide and in Puerto Rico because stability testing revealed an overfilled vial in a single lot.
Product
BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only BiCNU manufactured by: Ben Venue Laboratories, Inc. Bedford, OH 44146 Diluent manufactured by: Luitpold Pharmaceuticals, Inc. Shirley, NY 11967 Distributed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-024-2013·2012-10-31
Raritan Recalls Leader Fiber Capsules Due to C. Difficile Contamination
Raritan Pharmaceuticals is recalling Leader Fiber Capsules due to possible C. difficile contamination found in raw materials.
Product
Leader Fiber Capsules, 100% Natural Psyllium Fiber Laxative, Dietary Fiber Supplement, Relieves Constipation, Restores Regularity, 100 capsules per bottle, Distributed by: Cardinal Health, Dublin, OH 43017 www.myleader.com, NDC 37205-372-78, UPC 0-96295-11222-1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-016-2013·2012-10-31
Watson Recalls Necon 10/11 Tablets Due to Potential HCTZ Contamination
Watson Laboratories is recalling specific lots of Necon 10/11 oral contraceptives because they may contain trace amounts of Hydrochlorothiazide (HCTZ).
Product
Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP, 0.5 mg/35 mcg, 1 mg/35 mcg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA; Distributed by: Watson…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-027-2013·2012-10-31
Raritan Pharmaceuticals Recalls Wal-Mucil Plus Calcium Fiber Capsules
Raritan Pharmaceuticals is recalling Wal-Mucil Plus Calcium Fiber Capsules due to possible C. difficile contamination found in raw materials.
Product
Wal-Mucil Plus Calcium Fiber Capsules,100% Natural Fiber, 100% Natural Psyllium Seed Husk, Calcium/Dietary Fiber Supplement, 240 Capsules per bottle, Distributed by: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015-4616 www.walgreens.com, NDC 0363-0128-24, UPC 3-11917-07656-0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-030-2013·2012-10-31
Raritan Pharmaceuticals Recalls Premier Value Fiber Capsules Due to C. Difficile Contamination
Raritan Pharmaceuticals is recalling Premier Value Fiber Capsules due to possible C. difficile contamination found in the raw material.
Product
Premier Value Fiber Capsules, Fiber Capsules, 100% Natural Psyllium Fiber, Relieves Constipation, Restores Regularity, 160 Capsules per bottle, Distributed by: Chain Drug Consortium, LLC, Boca Raton, FL 33431, UPC0-40986-01703-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-033-2013·2012-10-31
Mylan Recalls Doxazosin Tablets Due to Acetaminophen and Codeine Contamination
Mylan Pharmaceuticals is recalling 24,331 bottles of Doxazosin Tablets, USP, 2 mg, due to cross-contamination with acetaminophen and codeine.
Product
Doxazosin Tablets, USP, 2 mg, 100 count bottles, labeled in part ***Manufactured in Australia by: ALPHAPHARM PTY LTD, 15 Garnet Street***Rx Only*** Carole Park QLD 4300, Australia*** Manufactured for Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.SA ***
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-017-2013·2012-10-31
Watson Recalls Necon 1/35-28 Tablets Due to Potential Cross-Contamination
Watson Laboratories is recalling Necon 1/35-28 tablets because certain lots may contain trace amounts of Hydrochlorothiazide (HCTZ). The recall covers 6,466 cartons distributed nationwide and in Puerto Rico.
Product
Necon 1/35-28 (norethindrone and ethinyl estradiol) Tablets USP, 1 mg/35 mcg, inert tablets, 28-count tablets per dispenser packaged in 6 Tablet Dispensers per carton, Rx only, Manufactured by: Watson Pharma, Inc., A subsidiary of Watson Pharmaceuticals, Inc., Corona, CA 92880…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-022-2013·2012-10-31
CVS Pharmacy Fiber Capsules Recalled for Possible C. Difficile Contamination
Raritan Pharmaceuticals is recalling CVS Pharmacy Fiber Capsules due to possible C. difficile contamination found in raw materials.
Product
CVS Pharmacy Fiber Capsules for Regularity, Dietary Fiber Supplement, 100 Capsules per bottle, Distributed by: CVS Pharmacy, Inc., Woonsocket, RI 02895 www.cvs.com UPC 0-50428-07739-9
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-029-2013·2012-10-31
Raritan Recalls Fiber Capsules Due to Possible C. Difficile Contamination
Raritan Pharmaceuticals is recalling Simply Right Healthcare Fiber Capsules due to possible C. difficile contamination found in raw materials.
Product
Simply Right Healthcare Fiber Capsules, 100% Natural Psyllium Fiber, Fiber Supplement, Fiber Laxative for Regularity, 400 capsules per bottle, Distributed by: SAM'S West, Inc., Bentonville, AR 72716, UPC 0-78742-00524-9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-025-2013·2012-10-31
Raritan Recalls Up&Up Psyllium Fiber Supplement for C. Difficile Contamination
Raritan Pharmaceuticals is recalling Up&Up Psyllium Fiber Supplement due to possible C. difficile contamination in the raw material.
Product
Up&Up Psyllium Fiber Supplement, 100% natural psyllium husk, Fiber Therapy for Regularity/Fiber Supplement, 160 capsules per bottle, Distributed by: Target Corp., Minneapolis, MN 55403, Made in USA, NDC 11673-059-87, UPC 3-68163-11926-8.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-032-2013·2012-10-31
Raritan Pharmaceuticals Recalls DRxChoice Fiber Capsules Due to Microbial Contamination
Raritan Pharmaceuticals is recalling DRxChoice Fiber Capsules due to possible C. difficile contamination found in raw materials.
Product
DRxChoice Fiber Capsules, 25 capsules per bottle, Psyllium Husk Fiber, Mfg. by Raritan Pharmaceuticals, East Brunswick, NJ, UPC 3-68163-11925-1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-028-2013·2012-10-31
Raritan Pharmaceuticals Recalls Fiber Capsules Due to Microbial Contamination
Raritan Pharmaceuticals is recalling Berkley & Jensen Fiber Capsules due to possible C. difficile contamination found in raw materials.
Product
Berkley & Jensen Fiber Capsules, Fiber Laxative/Fiber Supplement, 100% Natural Psyllium Fiber, 400 capsules per bottle, Distributed by: BJWC, 25 Research Drive, Westborough, MA 01581, Made in USA, UPC 4-00016-27053-2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-021-2013·2012-10-31
Psyllium Fiber Supplement Recalled for Possible C. Difficile Contamination
Raritan Pharmaceuticals is recalling Best Choice Health Care Psyllium Fiber Supplement due to possible C. difficile contamination in raw materials.
Product
Best Choice Health Care, Psyllium Fiber Supplement, 100% natural Psyllium Fiber Laxative, 100 capsules per bottle, Proudly Distributed by: Valu Merchandisers, Co., Kansas City, KS 06106, UPC 0-70038-63439-3
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-026-2013·2012-10-31
Raritan Pharmaceuticals Recalls Wal-Mucil Fiber Laxative Due to Microbial Contamination
Raritan Pharmaceuticals is recalling specific lots of Wal-Mucil fiber laxative capsules due to possible C. difficile contamination in the raw material.
Product
Wal-Mucil 100% Natural Fiber, 100% Natural Psyllium Seed Husk, Fiber Laxative/Supplement, a)160 capsules per bottle (item #503663), and b) 320 capsules per bottle (Item #586143), Distributed by: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015-4616, www.walgreens.com, a) UPC…
Category
Drug
Distribution
Distributed nationwide

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17676–17700 of 18050