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

9076–9100 of 17772

ModerateFDA (Drugs)·D-0050-2019·2018-10-24
Product Quest Recalls QC Quality Choice Saline Nasal Spray for CGMP Deviations
Product Quest Manufacturing LLC is recalling QC Quality Choice Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
QC Quality Choice, Saline Nasal Relief, Moisturizing Nasal Spray, Sodium Chloride 0.65%, packaged as a) 1.5 FL OZ (45 mL) bottle UPC 6 35515 98845 3; b) 3 FL OZ (89 mL) bottle UPC 6 35515 95042 9, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0032-2019·2018-10-24
CVS Health Sterile Saline Nasal Mist Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling CVS Health Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
CVS Health, Sterile Saline Nasal Mist (sodium chloride) Allergy & Sinus Relief, 3.0%, 4.25 OZ (126 g) can, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 41854 3.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0037-2019·2018-10-24
Product Quest Recalls DG Health Nasal Pump Mist for CGMP Deviations
Product Quest Manufacturing LLC is recalling 786,720 bottles of DG Health No Drip Nasal Pump Mist due to manufacturing deviations that could impact product quality.
Product
DG health, No Drip, Nasal Pump Mist (oxymetazoline hydrochloride), 0.05%, 1 FL OZ (30 mL) bottle, Distributed by: Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072, UPC 7 27510 00373 3 .
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0041-2019·2018-10-24
Product Quest Recalls Meijer Saline Nasal Spray Due to Quality Deviations
Product Quest Manufacturing LLC is recalling Meijer Saline Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
meijer, Saline Nasal Spray, Nasal Moisturizing Spray, packaged as a) 1.5 FL OZ (44 mL) UPC 7 08820 74428 8; b) 3FL OZ (88 mL) UPC 7 08820 74430 1, Dist. By Meijer Distribution, Inc., Grand Rapids, MI 49544 .
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0052-2019·2018-10-24
Thayers Saline Nasal Mist Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing is recalling Thayers Saline Nasal Mist due to manufacturing conditions that could impact product quality.
Product
Thayers Natural Remedies, Saline Nasal Mist, Allergy & Sinus Relief, Slippery Elm, 3 FL OZ (89 mL) can, Distributed By: Product Quest Manufacturing, LLC, 330 Carswell Ave., Daytona Beach, FL 32117, UPC 7 27510 00659 8.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0040-2019·2018-10-24
Harmon Face Values Saline Nasal Spray Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling Harmon Face Values Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Harmon Face Values, Saline Nasal Spray (sodium chloride), 0.65%, packaged as a) 1.5 FL OZ (44 mL) bottle UPC 7 27510 00501 0; b) 3 FL OZ (88 mL) bottle UPC 7 27510 00502 7, Distributed by Harmon Stores, Inc., Union, NJ 07083 USA.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2019·2018-10-24
Walgreens Severe Anefrin Nasal Spray Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling Walgreens NO DRIP Severe Anefrin Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Walgreens, NO DRIP Severe Anefrin Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour + Menthol, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7001-01, UPC 3 11917 18536 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0059-2019·2018-10-24
Product Quest Recalls Best Choice Saline Nasal Spray for Quality Deviations
Product Quest Manufacturing LLC is recalling Best Choice Saline Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
Best Choice, SALINE Nasal Spray (Sodium Chloride 0.65% Phenylcarbinol & Benzalkonium Chloride as Preservatives), 1.5 FL OZ (44 mL) bottle, Proudly Distributed By: Valu Merchandisers, Co., 5000 Kansas Ave, Kansas City, KS 66106, UPC 0 70038 58487 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0056-2019·2018-10-24
FDA Recalls Best Choice Nasal Spray Due to Manufacturing Deviations
Product Quest Manufacturing LLC is recalling Best Choice Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
Best Choice, 12 Hour Extra Moisturizing, Nasal Spray (Oxymetazoline Hydrochloride 0.05%), Nasal Decongestant, 1 FL OZ (30 mL) bottle, Proudly Distributed By: Valu Merchandisers, Co., 5000 Kansas Ave., Kansas City, KS 66106, UPC 0 70038 59328 7.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0033-2019·2018-10-24
CVS Health Baby Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling CVS Health Baby Nasal Spray/Drops due to manufacturing conditions that could impact product quality.
Product
CVS Health, Baby Nasal Spray/Drops, Non-Medicated, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 29380 5 Product #459367.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0038-2019·2018-10-24
Product Quest Recalls Saline Nasal Mist Due to Manufacturing Deviations
Product Quest Manufacturing LLC is recalling 46,056 cans of FAMILY wellness Sterile Saline Nasal Mist because they were manufactured under conditions that could impact product quality.
Product
FAMILY wellness, Sterile Saline, Nasal Mist, Saline Nasal Relief (0.9% Sodium Chloride Solution), 4.25 FL OZ (126 mL) can, Distributed by: Midwood Brands, LLC, 10611 Monroe Rd., Matthews, NC 28105, UPC 0 32251 11617 9.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0034-2019·2018-10-24
CVS Saline Nasal Gel Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling CVS Health Saline Nasal Gel with Soothing Aloe due to manufacturing conditions that could impact product quality.
Product
CVS Health, Saline Nasal Gel with Soothing Aloe, packaged as a) Baby Net Wt. 0.5 OZ (14.2 g) tube UPC 0 50428 58392 0 Product #282476; and b) Net Wt. 0.5 OZ tube (14.2 g) UPC 0 50428 31746 4 Product #896071; Distributed by CVS Pharmacy, Inc,. One CVS Drive, Woonsocket, RI 02895.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0078-2019·2018-10-24
Rexall Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Rexall Extra Moisturizing No Drip Nasal Spray due to manufacturing conditions that could impact product quality.
Product
Rexall, Extra Moisturizing No Drip Nasal Spray (Oxymetazoline Hydrochloride 0.05%) 1 FL OZ (30 mL) bottle, 48 pk. (12687901)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0067-2019·2018-10-24
Rite Aid First Aid Antibiotic Ointment Recalled for Low Bacitracin Zinc
Product Quest Manufacturing LLC is recalling Rite Aid First Aid Antibiotic Ointment because the bacitracin zinc ingredient was found to be subpotent.
Product
Rite Aid Pharmacy, First Aid Antibiotic Ointment, (neomycin sulfate 3.5 mg, polymyxin B sulfate 5,000 units, bacitracin zinc 400 units per gram), 2 OZ (56 g) tube, Distributed By: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011, UPC 0 11822 55441 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0060-2019·2018-10-24
Walgreens Nasal Decongestant Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Walgreens Nasal Spray (Oxymetazoline HCl 0.05%) due to CGMP deviations that could impact product quality.
Product
Walgreens, Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour, 0.75 FL OZ (22 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015, UPC 3 11917 18622 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0046-2019·2018-10-24
Premier Value Sterile Saline Nasal Mist Recalled for Quality Concerns
Product Quest Manufacturing LLC is recalling 10,584 cans of Premier Value Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
Premier Value, Sterile Saline Nasal Mist, Saline Nasal Moisturizer (0.9% Sodium Chloride) Solution, 4.25 FL OZ (126 mL) can, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca Raton, FL 33431, NDC 8 40986 02998 1.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0070-2019·2018-10-24
Cicatricure Scar Cream Recalled for Low Active Ingredient Levels
Product Quest Manufacturing LLC is recalling Cicatricure Scar Cream + Sunscreen SPF 30 because the octocrylene and avobenzone levels were found to be lower than required.
Product
Cicatricure, Scar Cream + Sunscreen SPF 30 (avobenzone 3%, octocrylene 10%, oxybenzone 6%), 0.7 oz. (19.8 g) tube, Distributed by: Genomma Lab USA Inc., Houston, TX 77027, UPC 6 50067 00018 7.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0025-2019·2018-10-24
Mylan Recalls Levonorgestrel and Ethinyl Estradiol Tablets Due to Labeling Errors
Mylan Pharmaceuticals is recalling specific lots of levonorgestrel and ethinyl estradiol tablets because the blister packs display incorrect NDC and product name information.
Product
Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg/0.03 mg, Rx Only, 3 extended-cycle blister packs containing 91 tablets each, Made in India, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-7281-53.
Category
Drug
Distribution
0 states
LowFDA (Drugs)·D-0069-2019·2018-10-24
Well at Walgreens Scar Cream Recalled for Low Active Ingredient Levels
Product Quest Manufacturing LLC is recalling 6,516 tubes of Well at Walgreens Scar Cream with SPF 30 because the octocrylene and avobenzone levels were found to be lower than required.
Product
Well at Walgreens, Scar Cream with SPF 30, (Avobenzone 3%, Octocrylene 10%, Oxybenzone 6%), 0.7 OZ (19.8 g) tube, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, UPC 3 11917 18281 0.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0249-2019·2018-10-24
Amerigen Recalls Temozolomide Capsules Due to Dissolution Failures
Amerigen Pharmaceuticals is recalling Temozolomide capsules because stability testing revealed out-of-specification dissolution results.
Product
Temozolomide capsules, 20 mg, packaged in a) 5-count bottle(NCD 43975-253-05), b) 14-count bottle (NDC 43975-253-14), Rx only, Mfd. by: Stason Pharmaceuticals, Inc., Irvine, CA 92618, Dist. By: Amerigen Pharmaceuticals, Lyndhurst, NJ 07071.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0015-2019·2018-10-17
Magnesium Sulfate Injection Recalled Due to Mispackaged Heparin Unit
Pfizer is recalling 94,752 bags of Magnesium Sulfate in Water for Injection because a single unit of Heparin was found inside a case.
Product
MAGNESIUM SULFATE IN WATER — MAGNESIUM SULFATE IN WATER (MAGNESIUM SULFATE IN WATER)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0008-2019·2018-10-17
Alkano Chemicals Recalls Thyroid Powder Due to Inconsistent Active Ingredient Levels
Alkano Chemicals, Inc. is recalling 8 kg of Thyroid Powder, Lot # 170501, due to inconsistent levels of active ingredients levothyroxine and liothyronine.
Product
Thyroid powder, 4.5 kg foil bag, 5x1 kg foil bags packed in 25 Kg Fiber Drum, Thyroid Powder 25kg/drum, US Pharmacopoeia, Sichuan Friendly Pharmaceutical Co., LTD, Production Address: No. 680, Hongpai Road, Dongxing District, Neijiang City Sichuan, China Tel:+886 832 2240082/2240
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0010-2019·2018-10-17
Pfizer Recalls Glipizide XL Tablets Due to Manufacturing Deviations
Pfizer is recalling 7,777 bottles of Glipizide XL 5 mg tablets because rejected product was used in manufacturing, violating CGMP standards.
Product
Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC. Peapack, NJ 07977 --- NDC 59762-0541-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0011-2019·2018-10-17
Jubilant Cadista Recalls Pantoprazole Tablets Due to Dark Discoloration
Jubilant Cadista Pharmaceuticals is recalling 158,466 bottles of 40 mg pantoprazole sodium delayed-release tablets due to dark discoloration or brown spots on the edges.
Product
Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801; NDC 59746-284-90.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0088-2019·2018-10-17
GSK Recalls Prevacid 24HR Capsules Due to Manufacturing Deviations
GSK is voluntarily recalling Prevacid 24HR capsules nationwide due to Current Good Manufacturing Practice (CGMP) deviations. No illnesses have been reported.
Product
Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.
Category
Drug
Distribution
Distributed nationwide

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9076–9100 of 17772