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

4126–4150 of 5062

ModerateFDA (Drugs)·D-0651-2022·2022-03-16
Alprazolam 2 mg tablets recalled due to potential cross-contamination
Direct Rx is recalling Alprazolam C-IV 2 mg tablets (Lot #07NO1901, expiration 5/31/22) distributed in Florida, Georgia, and Louisiana due to potential cross-contamination identified at the contract manufacturer Ultra Tab Laboratories Inc.
Product
Alprazolam C-IV 2 mg, 60-count bottles, Rx Only, Dist. By: Par Pharmaceutical Chestnut Ridge, NY 10977 Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 72189-0058-60
Category
Drug
Distribution
3 states
ModerateFDA (Drugs)·D-0642-2022·2022-03-09
Alprazolam Tablets 1mg Recalled for CGMP Deviations
Preferred Pharmaceuticals is recalling 276 bottles of Alprazolam Tablets USP 1mg (generic Xanax) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall was initiated voluntarily by the manufacturer.
Product
Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) 30 tablets per bottle, NDC: 68788-6381-03, b) 60 tablets per bottle, NDC: 68788-6381-06, c) 90 tablets per bottle, NDC: 68788-6381-09, Mfg: Par Pharmaceutical.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0636-2022·2022-03-09
TSM Brands Isopropyl Alcohol Recalled for Undeclared Ethyl Alcohol
TSM Brands LLC is recalling Luxury 70% Isopropyl Alcohol bottles nationwide because the product contains undeclared ethyl alcohol that is not identified on the label.
Product
Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1PT) 473 ML bottle, Distributed by: TSM Brands LLC, 540 Equinox Ln, Manalapan, NJ 07726, UPC 868275965734.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0641-2022·2022-03-09
Over-The-Counter Drug Products Sold by Family Dollar Stores Recalled
Dollar Tree Distribution is recalling all over-the-counter drug products sold by Family Dollar retail stores in six states due to potential rodent exposure at a distribution center.
Product
All Over-The-Counter (OTC) drug products sold by Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and Tennessee.
Category
Drug
Distribution
0 states
ModerateFDA (Drugs)·D-0639-2022·2022-03-09
Olanzapine 10 mg tablets recalled due to cGMP deviations
Macleods Pharma USA is voluntarily recalling Olanzapine 10 mg tablets nationwide due to cGMP (current good manufacturing practices) deviations identified during manufacturing. The recall affects 3,672 bottles distributed across the United States.
Product
OLANZAPINE — OLANZAPINE (OLANZAPINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0637-2022·2022-03-09
Moxifloxacin Ophthalmic Solution Recalled for Failed Impurity Specifications
Direct Rx is recalling Moxifloxacin Ophthalmic Solution USP 0.5% due to failed impurities and degradation specifications. The recall affects 44 bottles distributed in Florida.
Product
Moxifloxacin Ophthalmic Solution USP 0.5%, 3 mL, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 Dist. By Aurobindo Pharma USA, Inc. East Windsor, NJ 08520, NDC 72189-076-05
Category
Drug
Distribution
0 states
ModerateFDA (Drugs)·D-0635-2022·2022-03-09
70% Isopropyl Alcohol First Aid Antiseptic Contains Undeclared Ethyl Alcohol
TSM Brands LLC is recalling 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen due to undeclared ethyl alcohol in the product. The recall affects bottles distributed nationwide.
Product
70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML bottle, Distributed By: TSM Brands LLC, 540 Equinox LN, Manalapan, NJ 07726, www.tsmbrands.com, Made in Turkey, UPC 868275965765
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0632-2022·2022-03-09
Amlodipine and Olmesartan Medoxomil Tablets Recalled for cGMP Deviations
Macleods Pharma USA is recalling one lot of Amlodipine and Olmesartan Medoxomil Tablets nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and was initiated by the manufacturer.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0713-2022·2022-03-09
Dexamethasone Elixir Recalled for Impurities Above Permissible Levels
Morton Grove Pharmaceuticals is recalling Dexamethasone Elixir USP 0.5 mg/5 mL nationwide due to unknown impurities found at higher than permissible levels in affected lots.
Product
Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0644-2022·2022-03-09
HEB Isopropyl Alcohol First Aid Antiseptic Label Mix-Up Recall
HEB 50% Isopropyl Alcohol First Aid Antiseptic bottles contain 3% Hydrogen Peroxide instead due to a label mix-up. The front label incorrectly identifies the product as isopropyl alcohol when the contents are actually a hydrogen peroxide topical solution.
Product
HEB 50% Isopropyl Alcohol First Aid Antiseptic, packaged in 16 FL OZ 91 PT) 473 mL brown bottles with brown colored closures. Distributed by HEB San Antonio, TX 78204. UPC 0 41220 25111 7
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-0645-2022·2022-03-02
RISE UP RED EDITION Capsules recalled for undeclared tadalafil
RISE UP RED EDITION Capsules, 650 mg, have been recalled because they contain undeclared tadalafil, an ingredient found in FDA-approved male sexual enhancement products. The product is an unapproved drug and was distributed nationwide via Amazon Marketplace.
Product
RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0602-2022·2022-03-02
Good Sense Children's Pain and Fever acetaminophen oral suspension recall
Perrigo is recalling Good Sense Children's Pain and Fever acetaminophen oral suspension (160 mg/5 ml) in 4 FL OZ bottles due to contaminated excipient used during manufacturing. The recalled batch 1CK0963 (expiration 12/31/2022) was distributed nationwide.
Product
GOOD SENSE CHILDRENS PAIN AND FEVER — GOOD SENSE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2022·2022-03-02
Perrigo Nasal Spray Recalled for Contaminated Excipient
Perrigo Company PLC is recalling NASAL Maximum Strength Nasal Spray (oxymetazoline HCl 0.05%) due to manufacturing with a contaminated excipient that was itself recalled from the supplier. The recall affects one batch distributed nationwide.
Product
NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0619-2022·2022-03-02
Perrigo Nasal Oxymetazoline Spray Recalled for Contaminated Excipient
Perrigo Company PLC is recalling approximately 10,800 bottles of NASAL Maximum Strength No Drip Nasal Spray (Oxymetazoline HCl 0.05%) nationwide due to manufacturing with a contaminated excipient supplied by their ingredient vendor.
Product
NASAL — NASAL (OXYMETAZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0584-2022·2022-03-02
UP AND UP Acetaminophen Infant Suspension Recalled for Contaminated Excipient
Perrigo Company PLC is recalling UP AND UP Acetaminophen Infant Dye Free Grape Oral Suspension due to use of a contaminated excipient supplied by an outside vendor. The product was distributed nationwide.
Product
UP AND UP ACETAMINOPHEN — UP AND UP ACETAMINOPHEN (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0628-2022·2022-03-02
Nasal Spray Oxymetazoline HCl Recalled Due to Contaminated Excipient
Perrigo Company PLC is recalling Nasal Maximum Strength Nasal Spray (Oxymetazoline HCl 0.05%) due to contamination from a recalled excipient used during manufacturing. Approximately 2,302 bottles were distributed nationwide.
Product
NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0570-2022·2022-03-02
Prevantics Maxi Swabstick Recall Due to Manufacturing Validation Issues
Professional Disposables International is recalling Prevantics Maxi Swabstick (chlorhexidine gluconate and isopropyl alcohol) due to unvalidated test methods used during manufacturing. The company has not reported any illnesses or injuries.
Product
PREVANTICS MAXI SWABSTICK — PREVANTICS MAXI SWABSTICK (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0624-2022·2022-03-02
Oxymetazoline Nasal Spray Recalled for Contaminated Excipient
Perrigo Company is recalling Maximum Strength No Drip Nasal Spray containing oxymetazoline HCl because it was manufactured with a contaminated excipient obtained from a recalled supplier.
Product
NASAL — NASAL (OXYMETAZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0588-2022·2022-03-02
Children's Acetaminophen Oral Suspension Recall due to Contaminated Excipient
Perrigo Company is recalling Children's Pain and Fever (Acetaminophen) Oral Suspension distributed by Kroger nationwide due to manufacturing with a contaminated excipient. The product was made with an ingredient sourced from a supplier that had recalled that same excipient.
Product
CHILDRENS PAIN AND FEVER — CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0582-2022·2022-03-02
Children's Cherry Acetaminophen Oral Suspension Recalled for Contaminated Excipient
Perrigo is recalling Children's Cherry Flavored Acetaminophen Oral Suspension (160mg/5ml) because the product was manufactured with a contaminated excipient that was recalled from the supplier.
Product
Children's Cherry Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 45802-203-26
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0610-2022·2022-03-02
Equaline Nasal Spray Recalled for Contaminated Excipient
Perrigo Company is recalling Equaline Nasal Spray (oxymetazoline HCl 0.05%) due to manufacturing with a contaminated excipient obtained from a recalled supplier. The recall affects approximately 2,664 bottles distributed nationwide.
Product
EQUALINE NASAL — EQUALINE NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0618-2022·2022-03-02
Soothing 12 Hour Nasal Decongestant Spray Recall Due to Contaminated Excipient
Perrigo Company PLC is recalling Soothing 12 Hour Nasal Decongestant Spray nationwide because the product was manufactured with a contaminated excipient that was recalled from the supplier.
Product
Soothing 12 Hour Nasal Decongestant Spray No Drip, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Distributed By MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152. NDC 0904-6761-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0575-2022·2022-03-02
Dr. Reddy's Azacitidine Injectable Drug Recalled for Failed Stability
Dr. Reddy's Laboratories is recalling Azacitidine 100mg injectable vials nationwide due to failed stability specifications. Multiple lot numbers distributed across the United States are affected.
Product
AZACITIDINE — AZACITIDINE (AZACITIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0616-2022·2022-03-02
DG Health Nasal Spray Recalled for Contaminated Excipient
Perrigo Company is recalling DG Health Nasal (Oxymetazoline Hydrochloride) nasal spray because it was manufactured with a contaminated excipient obtained from a recalled supplier.
Product
DG HEALTH NASAL — DG HEALTH NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0603-2022·2022-03-02
Basic Care No Drip Nasal Spray Recalled for Contaminated Excipient
Perrigo Company is recalling 37,104 bottles of Basic Care No Drip Nasal Spray (oxymetazoline hydrochloride 0.05%) nationwide due to contaminated excipient used during manufacturing. The affected batches were distributed to U.S. consumers.
Product
BASIC CARE NO DRIP NASAL — BASIC CARE NO DRIP NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide

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4126–4150 of 5062