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

10001–10025 of 114051

ModerateFDA (Food)·F-0701-2025·2025-04-16
Desert Farms Jalapeno Mustard Recalled for Processing Defect
The Truck Farm, LLC is recalling Desert Farms Jalapeno Mustard nationwide due to lack of an approved filed process and missing monitoring records. This is a Class II recall by the FDA.
Product
Desert Farms Jalapeno Mustard. Caution to refrigerate after opening. The shelf life is 2 years after the date of manufacture. It is packaged in 8 oz glass jars with a net wt. of 8.8 oz (249g). UPC code 05423401721, The Truck Farm, LLC 645 S. Alameda Las Cruces, NM, 88005.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1540-2025·2025-04-16
Stryker Blueprint Mixed Reality Depth Stop Pin Total Shoulder Arthroplasty Recalled
Stryker is recalling the Blueprint Mixed Reality Depth Stop Pin (Catalog Number MRUE206) due to elevated complaints of software and instrumentation malfunctions that prevent intended use. The recall affects 474 units distributed in multiple US states and internationally.
Product
stryker Blueprint Mixed Reality Depth Stop Pin, Catalog Number MRUE206; Total Shoulder Arthroplasty
Category
Medical Device
Distribution
7 states
ModerateFDA (Drugs)·D-0346-2025·2025-04-16
Naproxen Sodium tablets recalled due to manufacturing compliance deviations
Glenmark Pharmaceuticals Inc., USA is recalling Naproxen Sodium Tablets, USP 550mg nationwide due to CGMP (Current Good Manufacturing Practice) deviations identified during manufacturing. The recall affects lot #17231956 with expiration date Aug-25.
Product
NAPROXEN SODIUM — NAPROXEN SODIUM (NAPROXEN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0315-2025·2025-04-16
Propafenone Hydrochloride Extended-Release Capsules Recalled for CGMP Deviations
Glenmark Pharmaceuticals Inc., USA is recalling Propafenone Hydrochloride Extended-Release Capsules 225mg due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects lot #17230819 with expiration date March 2025, distributed nationwide.
Product
PROPAFENONE HYDROCHLORIDE — PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0325-2025·2025-04-16
Glenmark Pharmaceuticals Recalls Pravastatin Sodium Tablets 80mg
Glenmark Pharmaceuticals Inc., USA is recalling specific lots of Pravastatin Sodium Tablets 80mg due to Current Good Manufacturing Practice (CGMP) deviations. The recall applies to affected lots distributed nationwide and was initiated voluntarily by the firm.
Product
PRAVASTATIN SODIUM — PRAVASTATIN SODIUM (PRAVASTATIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0318-2025·2025-04-16
Prescription Voriconazole Antifungal Tablets Recalled Nationwide for Manufacturing Deviations
Glenmark Pharmaceuticals is voluntarily recalling Voriconazole tablets nationwide due to manufacturing process deviations. No illnesses or injuries have been reported.
Product
VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0697-2025·2025-04-16
Cabot Creamery Extra Creamy Premium Butter Recalled for Coliform Contamination
Cabot Creamery 8oz Extra Creamy Premium Sea Salted Butter is recalled due to contamination with elevated levels of coliform. The affected product was distributed in Vermont, New York, Pennsylvania, Maine, Connecticut, New Hampshire, and Arkansas.
Product
Cabot Creamery 8oz Extra Creamy Premium Butter, Sea Salted. Packaged as (2) 4oz sticks in cardboard shells; UPC: 0 78354 62038 0
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-0353-2025·2025-04-16
Sodium Chloride Irrigation Solution Recalled for Particulate Matter
B. Braun Medical Inc. is recalling a sodium chloride irrigation solution due to the presence of particulate matter. The product was distributed to 12 distributors who may have further distributed it nationwide.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0313-2025·2025-04-16
Sofosbuvir and Velpatasvir Tablets Recalled for Defective Blister Pack Sealing
Asegua Therapeutics is recalling 18,541 cartons of Sofosbuvir and Velpatasvir tablets nationwide due to defective blister packs that are not properly sealed, resulting in loose tablets in cartons. No illnesses or injuries have been reported.
Product
SOFOSBUVIR AND VELPATASVIR — SOFOSBUVIR AND VELPATASVIR (VELPATASVIR AND SOFOSBUVIR)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0333-2025·2025-04-16
Solifenacin Succinate Tablets Recalled Due to Manufacturing Deviations
Glenmark Pharmaceuticals Inc., USA is recalling Solifenacin Succinate 5mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and affects 30-count and 90-count bottles distributed across the U.S.
Product
SOLIFENACIN SUCCINATE — SOLIFENACIN SUCCINATE (SOLIFENACIN SUCCINATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0317-2025·2025-04-16
Solifenacin succinate tablets recalled nationwide for manufacturing practice deviations
Glenmark Pharmaceuticals is recalling solifenacin succinate 10mg tablets nationwide due to manufacturing process deviations. The voluntary recall affects specific lot numbers distributed across the United States.
Product
SOLIFENACIN SUCCINATE — SOLIFENACIN SUCCINATE (SOLIFENACIN SUCCINATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0339-2025·2025-04-16
Rosuvastatin Calcium Tablets Recalled Nationwide Due to Manufacturing Deviations
Glenmark Pharmaceuticals is voluntarily recalling Rosuvastatin Calcium 40mg tablets nationwide due to manufacturing practice deviations. The recall affects specific lot numbers expiring February through June 2026.
Product
ROSUVASTATIN CALCIUM — ROSUVASTATIN CALCIUM (ROSUVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0319-2025·2025-04-16
Voriconazole Tablets 50mg Recalled Due to CGMP Deviations
Glenmark Pharmaceuticals Inc. USA is recalling Voriconazole Tablets 50mg (Lot # 17231045, exp. date Apr-25) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing.
Product
VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0316-2025·2025-04-16
Propafenone Hydrochloride Extended-Release Capsules Recalled for CGMP Deviations
Glenmark Pharmaceuticals Inc. is recalling Propafenone Hydrochloride Extended-Release Capsules 325mg (Lot #17230767, expiring Mar-25) distributed nationwide due to current Good Manufacturing Practice (CGMP) deviations. Patients taking this medication should consult their physician before discontinuing use.
Product
PROPAFENONE HYDROCHLORIDE — PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0338-2025·2025-04-16
Prochlorperazine Maleate Tablets Recalled for Manufacturing Process Deviations
Glenmark Pharmaceuticals is voluntarily recalling Prochlorperazine Maleate 10mg tablets (NDC# 68462-890-01) distributed nationwide due to manufacturing process deviations. No illnesses or injuries have been reported.
Product
Prochlorperazine Maleate Tablets, 10mg, 100-count bottles, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for: Glenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430. NDC# 68462-890-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0696-2025·2025-04-16
Red Shell Teriyaki Sauce Recall Due to Microbial Growth
Red Shell branded Teriyaki Sauce is being recalled due to signs of microbial growth, including bubbling and swollen containers. The affected products were distributed primarily in California.
Product
Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benzoate), water, sugar, cooking wine( water, rice, malt), sweet cooking wine(corn syrup, rice, water, malt), modified food starch, dried onion, dried ginger root, dried garlic, lactic
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-0320-2025·2025-04-16
Gabapentin 600mg Tablets Recalled for CGMP Deviations
Glenmark Pharmaceuticals Inc. is voluntarily recalling Gabapentin 600mg tablets (500-count bottles) nationwide due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0326-2025·2025-04-16
Fluphenazine Hydrochloride Tablets Recalled for CGMP Deviations
Glenmark Pharmaceuticals Inc., USA is voluntarily recalling Fluphenazine Hydrochloride Tablets, 10mg due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects one lot distributed nationwide.
Product
FLUPHENAZINE HYDROCHLORIDE — FLUPHENAZINE HYDROCHLORIDE (FLUPHENAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0345-2025·2025-04-16
FDA Recalls Saxagliptin Tablets Due to Manufacturing Deviations
Glenmark Pharmaceuticals is recalling Saxagliptin 2.5mg tablets nationwide due to manufacturing quality issues. The firm initiated this voluntary recall on March 13, 2025.
Product
SAXAGLIPTIN — SAXAGLIPTIN (SAXAGLIPTIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0322-2025·2025-04-16
Frovatriptan Succinate tablets recalled due to manufacturing deviations
Glenmark Pharmaceuticals Inc., USA is recalling Frovatriptan Succinate 2.5mg tablets nationwide due to current Good Manufacturing Practice (CGMP) deviations. The FDA has classified this as a Class II recall.
Product
FROVATRIPTAN SUCCINATE — FROVATRIPTAN SUCCINATE (FROVATRIPTAN SUCCINATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0311-2025·2025-04-16
Gabapentin Capsules Recalled for Cross Contamination
Sun Pharmaceutical Industries is recalling Gabapentin Capsules, USP 300 mg, due to cross contamination. The recall affects approximately 12,876 bottles distributed nationwide.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0312-2025·2025-04-16
Gabapentin Capsules 400 mg Recalled for Cross Contamination
Sun Pharmaceutical Industries Inc. is recalling Gabapentin Capsules 400 mg due to cross contamination. The recall affects 852 bottles distributed nationwide.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25T006000·2025-04-15
Goodyear Recalls Cooper Tires Missing Identification Codes
Goodyear is recalling specific Cooper Discoverer Stronghold AT tires because they lack the required week and year code. This prevents owners from determining the tire's age or recall status.
Product
TIRES:MARKINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V246000·2025-04-15
Alfa Romeo Tonale and Dodge Hornet displays may omit rearview image
Chrysler is recalling certain 2023-2025 Alfa Romeo Tonale and Dodge Hornet vehicles because the display module may not show the rearview camera image, failing FMVSS 111.
Product
ALFA ROMEO — ALFA ROMEO, DODGE TONALE PHEV, TONALE, HORNET
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V227000·2025-04-15
Audi Recalls 2022-2023 E-TRON GT Models for Passenger Air Bag Fault
Audi is recalling 2022-2023 RS E-TRON GT and E-TRON GT vehicles because a wiring fault may deactivate the front passenger air bag, increasing injury risk in a crash.
Product
AUDI — AUDI RS E-TRON GT, E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide

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10001–10025 of 114051