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

3776–3800 of 5062

ModerateFDA (Drugs)·D-1069-2022·2022-06-15
Medroxyprogesterone acetate injection recalled due to temperature abuse manufacturing deviation
McKesson Medical-Surgical is recalling medroxyprogesterone acetate injectable suspension (150 mg/mL) due to temperature abuse during manufacturing. The affected vials were distributed nationwide; patients should contact their healthcare provider.
Product
Medroxyprogesterone acetate injectable suspension, USP, 150 mg/mL, 1 mL vials, packaged in a) single dose vial (NDC 0703-6801-01), b) 25-count box single dose vials (NDC 0703-6801-04), Rx only, MFG: Teva Pharma USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1078-2022·2022-06-15
Propofol Injectable Emulsion Recalled for Temperature Abuse During Manufacture
McKesson Medical-Surgical is recalling Teva Propofol Injectable Emulsion (200 mg/20 mL, 25-vial cartons) nationwide due to temperature abuse during manufacturing that may affect product quality. A total of 564 cartons were distributed.
Product
Propofol Injectable Emulsion, USP 200 mg per 20 mL (10 mg per mL), twenty-five 20 mL vials, Rx only, MFG: Teva Pharma USA, NDC 0591-2136-95
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0983-2022·2022-06-15
Xiidra ophthalmic solution recalled for failed impurity and degradation specifications
Novartis recalls approximately 1.25 million vials of Xiidra ophthalmic solution nationwide due to failed impurity and degradation specifications. Patients using this product should contact their healthcare provider.
Product
Xiidra (lifitegrast ophthalmic solution) 5%, packaged in a) 60 Single-Use Containers: 12 pouches x 5 single-use containers (0.2 mL each vial) (NDC 54092-606-01) and b) 5-Single-Use Containers (NDC 54092-606-06), Rx Only, Manufactured for: Shire US Inc., 300 Shire Way, Lexington,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1043-2022·2022-06-15
FDA Recalls Prescription Lidocaine Patch Due to Temperature Exposure
McKesson Medical-Surgical is recalling Lidocaine Patch 5% nationwide due to temperature abuse during distribution that may have compromised product quality. The FDA classified this as a Class II recall.
Product
LIDOCAINE — LIDOCAINE (LIDOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1047-2022·2022-06-15
FDA recalls Lidocaine-Prilocaine topical anesthetic cream for temperature abuse
McKesson Medical-Surgical is recalling Lidocaine and Prilocaine Cream due to cGMP deviations involving temperature abuse during distribution. The recall affects 23 tubes distributed nationwide.
Product
LIDOCAINE AND PRILOCAINE — LIDOCAINE AND PRILOCAINE (LIDOCAINE AND PRILOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1077-2022·2022-06-15
Propofol Injectable Emulsion Recalled for Temperature Abuse During Manufacturing
McKesson Medical-Surgical is recalling Propofol Injectable Emulsion vials due to cGMP manufacturing deviations involving temperature abuse. No illnesses have been reported.
Product
Propofol Injectable Emulsion, USP, 200 mg/ 20 mL (10 mg/mL), packaged in a) 50 mL vial, in packs of 20 (NDC 00591-2136-51), b) 100 mL vial, in packs of 10 (NDC 00591-2136-68), Rx only, MFG: Teva Pharma USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0988-2022·2022-06-15
FDA Recalls Teva Alprostadil Injection for Failed Impurity Specifications
Teva Pharmaceuticals USA Inc is recalling Alprostadil Injection USP due to out-of-specification results for impurities identified during routine stability testing. This FDA Class III recall affects 3,109 cartons distributed nationwide.
Product
Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-1501-02, Distributed by: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, Vial NDC 0703-1501-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1006-2022·2022-06-15
Arzol Silver Nitrate Applicator Recalled for Temperature-Related Manufacturing Defects
McKesson Medical-Surgical is recalling Arzol silver nitrate applicators nationwide due to temperature abuse during manufacturing that may affect product quality.
Product
Arzol (Silver Nitrate Applicator), (Silver Nitrate 75%, Potassium Nitrate 25%), 100-count box, Rx only, Manufacturer: Arzol Chemical Co, NDC 12870-0001-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0999-2022·2022-06-15
Bupivacaine Injectable Recalled for Temperature Abuse During Manufacturing
McKesson Medical-Surgical is recalling Bupivacaine HCl Injection vials (NDC 55150-0170-30) distributed nationwide due to temperature abuse during manufacturing that may affect product quality. No illnesses have been reported.
Product
Bupivacaine HCl Injection, single dose vial, 0.5%, 30 mL/5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0170-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1075-2022·2022-06-15
FDA Recalls Mupirocin Ointment Due to Temperature Control Deviations
Mupirocin Ointment distributed nationwide is being recalled due to temperature abuse violations during manufacturing. Consumers with affected supplies should contact their pharmacy or healthcare provider for guidance.
Product
MUPIROCIN — MUPIROCIN (MUPIROCIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1090-2022·2022-06-15
Proventil HFA albuterol inhalers recalled for manufacturing temperature deviation
Proventil HFA inhalers are being recalled nationwide by McKesson Medical-Surgical due to temperature abuse during manufacturing, a deviation from FDA Good Manufacturing Practice standards.
Product
Proventil HFA, (Albuterol Sulfate Inhalation Aerosol), 200 metered inhalations, Rx only, MFG: Merck Company, NDC 0085-1132-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1113-2022·2022-06-15
Tetracaine Hydrochloride Ophthalmic Solution Recalled for Temperature Abuse
McKesson Medical-Surgical is recalling Tetracaine Hydrochloride Ophthalmic Solution due to cGMP deviations from temperature abuse. The recall affects 43 cartons distributed nationwide.
Product
TETRACAINE HYDROCHLORIDE — TETRACAINE HYDROCHLORIDE (TETRACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1001-2022·2022-06-15
Bupivacaine HCl Injection Recalled for Temperature Control Deviation
McKesson Medical-Surgical is recalling Bupivacaine HCl Injection (0.50%, multi-dose vials, NDC 55150-0250-50) due to cGMP deviations related to temperature abuse during manufacturing. The product was distributed nationwide.
Product
Bupivacaine HCl Injection, Multi dose vial, 0.50%, 50 mL/5 mg/mL, Rx only, Manufacturer: Auromedics Pharma LLC, NDC 55150-0250-50
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1032-2022·2022-06-15
Doxycycline Capsules Recalled for Temperature Control Deviation
McKesson Medical-Surgical is recalling Doxycycline Capsules, USP, 100 mg due to temperature abuse during manufacturing. The Class II recall affects 3 bottles distributed nationwide across the USA.
Product
DOXYCYCLINE — DOXYCYCLINE (DOXYCYCLINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1036-2022·2022-06-15
FDA Recalls MIOSTAT Carbachol Solution Nationwide for Temperature Abuse
McKesson Medical-Surgical is recalling MIOSTAT (Carbachol Intraocular Solution) nationwide due to temperature abuse during distribution that may affect medication stability.
Product
MIOSTAT — MIOSTAT (CARBACHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1028-2022·2022-06-15
FDA Recalls Betamethasone Dipropionate Cream for Temperature-Abuse Storage Deviations
McKesson Medical-Surgical is recalling Betamethasone Dipropionate Cream USP 0.05% due to temperature-abuse cGMP deviations. The FDA Class II recall affects nationwide distribution.
Product
BETAMETHASONE DIPROPIONATE — BETAMETHASONE DIPROPIONATE (BETAMETHASONE DIPROPIONATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0992-2022·2022-06-08
Anagrelide Capsules Recalled Due to Failed Dissolution Specifications
Teva Pharmaceuticals is recalling Anagrelide Capsules USP 0.5 mg nationwide due to failed dissolution specifications discovered during stability testing. The recall involves lot GD01090 (expired May 2022).
Product
Anagrelide Capsules USP, 0.5 mg, 100-count bottles, Rx Only, Manufactured in India For: TEVA PHARMACEUTICALS USA, Inc., North Wales, PA 19454. NDC 0172-5241-60.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0973-2022·2022-06-08
Losartan Potassium Tablets Recalled for Elevated AZIDO Impurity Levels
Strides Pharma Inc. is recalling Losartan Potassium 50 mg tablets distributed nationwide due to AZIDO impurity levels exceeding acceptable FDA manufacturing standards.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0974-2022·2022-06-08
Losartan Potassium Tablets Recalled for CGMP Deviations and Elevated Impurity
Strides Pharma Inc. is recalling Losartan Potassium 100 mg tablets nationwide due to CGMP deviations with AZIDO impurity levels above acceptable limits. Patients should contact their healthcare provider to verify if they are affected.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0958-2022·2022-06-08
Injectable Hydromorphone Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection due to lack of assurance of sterility. The recall affects 6,210 pre-filled syringes distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL), 30 mL Pre-Filled Syringe, 5 x 30 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0969-2022·2022-06-08
Succinylcholine Chloride Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center LLC is recalling succinylcholine chloride injection due to lack of sterility assurance. The recall involves 181,560 pre-filled syringes distributed nationwide.
Product
Succinylcholine Chloride Injection, USP, 100 mg/5 mL (20 mg/mL), Preservative Free, 5 mL Pre-Filled Syringe, 5 x 5 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-920-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0957-2022·2022-06-08
Hydromorphone Injection Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Hydromorphone HCl Injection 50 mg/50 mL pre-filled syringes due to lack of sterility assurance. The recalled product was distributed nationwide.
Product
Hydromorphone HCl Injection, USP, 50 mg/50 mL (1 mg/mL), 50 mL Pre-Filled Syringe, 5 x 50 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-559-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0953-2022·2022-06-08
Nephron Epinephrine Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling 134,415 pre-filled syringes of Epinephrine Injection due to lack of assurance of sterility. Affected lots were distributed nationwide; patients and providers should contact their healthcare provider.
Product
Epinephrine Injection, USP, 1 mg/10 mL (100 mcg/mL), 10 mL Pre-Filled Syringe, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0965-2022·2022-06-08
Phenylephrine HCl Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center LLC is recalling Phenylephrine HCl Injection due to lack of assurance of sterility. Approximately 57,810 syringes were distributed nationwide.
Product
Phenylephrine HCl Injection, USP, 0.4 mg/10 mL (40 mcg/mL), 10 mL Pre-Filled Syringe, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-955-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0976-2022·2022-06-08
AMBI Skincare Fade Cream Recalled for Temperature Storage Deviations
AMBI Skincare Fade Cream is being recalled nationwide due to cGMP violations. The product was stored outside its labeled temperature requirements during manufacturing.
Product
AMBI Skincare Fade Cream Normal Skin, Net Wt. 2 OZ. (56g)
Category
Drug
Distribution
Distributed nationwide

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3776–3800 of 5062