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

7151–7175 of 89525

SevereFDA (Drugs)·D-0406-2025·2025-05-14
Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
BRS Analytical Services is recalling Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% eye lubricant nationwide due to cGMP deviations and lack of assurance of sterility. The recalled product was distributed in 0.5 FL OZ dropper bottles across multiple lots with various expiration dates in 2025 and 2026.
Product
CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0402-2025·2025-05-14
Ropivacaine Hydrochloride Injection Recalled for Particulate Matter
Amneal Pharmaceuticals is recalling Ropivacaine Hydrochloride Injection 0.5% due to the presence of particulate matter. The recall affects specific lots distributed nationwide.
Product
ROPIVACAINE HYDROCHLORIDE — ROPIVACAINE HYDROCHLORIDE (ROPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1717-2025·2025-05-14
CODMAN Craniotomy Kit Cranial Perforator Disposed Over Weld Defect
Integra LifeSciences is recalling CODMAN Craniotomy Kits due to inadequate welds that may cause the product to disassemble. The defect affects 1,840 units distributed worldwide.
Product
CODMAN Craniotomy Kit, Disposable Perforator Cranio-blade Wire Pass Drill, 14mm. Cranial perforator kit.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0404-2025·2025-05-14
Artificial Tears Eye Drops Recalled for Manufacturing and Sterility Issues
BRS Analytical Services is recalling Artificial Tears ophthalmic solution (0.5 FL OZ dropper bottles) nationwide due to manufacturing deviations and lack of assured sterility. Affected lots are Lot 126–129, 162–170, and 193–199.
Product
ARTIFICIAL TEARS — ARTIFICIAL TEARS (ARTIFICIAL TEARS)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0407-2025·2025-05-14
Lubricant Eye Drops Solution recalled due to sterility assurance concerns
BRS Analytical Services is recalling Lubricant Eye Drops Solution (Polyethylene Glycol 400 and Propylene Glycol) due to manufacturing deviations and lack of assurance of sterility. The product was distributed nationwide.
Product
LUBRICANT EYE DROPS SOLUTION — LUBRICANT EYE DROPS SOLUTION (POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0413-2025·2025-05-14
Testosterone Pellet 200 mg Recalled for Glass Particle Contamination
BSO LLC is recalling compounded testosterone pellets nationwide because glass particles were found in vials. Affected lot numbers are 20250207@1 and 20250228@1 (expiration 1/31/2026).
Product
TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0125-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1680-2025·2025-05-14
Intraocular Lenses enVista Envy and Envy Toric Recalled
Bausch & Lomb is recalling enVista Envy and enVista Envy Toric intraocular lenses due to increased reports of toxic anterior segment syndrome (TASS) following implantation.
Product
Intraocular Lens. enVista Envy IOL, All models starting with EN; enVista Envy Toric IOL, All models starting with ETN.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1716-2025·2025-05-14
CODMAN Disposable Cranial Perforator 14mm Recalled Due Weld Issue
Integra LifeSciences is recalling CODMAN Disposable Perforators (14mm) due to inadequate welds that could cause disassembly during use. The affected devices have been distributed worldwide.
Product
CODMAN Disposable Perforator, 14mm. Cranial perforator.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1682-2025·2025-05-14
CADD Solis VIP Ambulatory Infusion Pump Thermal Damage Recall
Smiths Medical is recalling CADD Solis VIP Ambulatory Infusion Pumps due to potential thermal damage. The recall affects 313,676 units distributed nationwide and worldwide.
Product
CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE, 1/EA, Model Number: 21-2127-0105-01; 2) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD ENABLED, 1/EA, Model Number: 21-2120-0105-01; 3) PUMP KI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0756-2025·2025-05-14
Bone & Joint Restore capsules recalled for potential salmonella contamination
Optimal Carnivore, LLC is recalling Bone & Joint Restore capsules nationwide due to potential contamination with salmonella. Consumers should stop using the product and contact the manufacturer.
Product
Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carnivore LLC 1603 Capitol Ave Ste 310 WY371 Cheyenne, WY 82001
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0762-2025·2025-05-14
Trader Joe's Sesame Miso Salad with Salmon recalled for undeclared milk
Taylor Farms Illinois Inc. is recalling Trader Joe's Sesame Miso Salad with Salmon (10.25 oz.) because it contains undeclared milk, which poses a risk to consumers with milk allergies.
Product
Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz., in clear plastic clamshell container, UPC 00773164
Category
Food
Distribution
18 states
SevereFDA (Drugs)·D-0408-2025·2025-05-14
Polyvinyl Alcohol Eye Drops Recalled for Manufacturing and Sterility Issues
BRS Analytical Services is recalling Polyvinyl Alcohol Ophthalmic Solution 1.4% eye drops nationwide due to cGMP deviations and lack of assurance of sterility.
Product
POLYVINYL ALCOHOL — POLYVINYL ALCOHOL (POLYVINYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0416-2025·2025-05-14
Testosterone Pellet 200 mg Recalled for Glass Particulate Matter
BSO LLC is recalling Testosterone Pellet 200 mg compounded drug vials nationwide because glass particles were found in the pellets intended for subcutaneous injection.
Product
TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0121-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0415-2025·2025-05-14
Testosterone Pellet 200 mg Recalled Due to Glass Particles
BSO LLC is recalling Testosterone Pellet 200 mg compounded drug vials nationwide due to the presence of glass particles found in pellet vials.
Product
TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0122-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0409-2025·2025-05-14
FentaNYL and Ropivacaine Epidural Injection Recalled Due to Sterility Concerns
Apollo Care, LLC is recalling FentaNYL 500mcg/2mcg/mL and Ropivacaine HCl 250mg/0.1% epidural injection due to lack of assurance of sterility. The recall affects 440 bags of a single lot distributed in Missouri.
Product
FentaNYL 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (0.1%) added to 250 mL, 0.9% Sodium Chloride Injection (For Epidural Use Only), Sterile, Single-Use Container, Rx Only, Apollocare, 3801 Mojave Ct, Ste 101, Columbia, MO 65202, NDC 71170-950-25
Category
Drug
Distribution
1 state
HighFDA (Food)·F-0761-2025·2025-05-14
Ankimo branded Monkfish Liver recalled for undeclared milk allergen
Ankimo branded Monkfish Liver (7 oz) is recalled because it contains undeclared milk, a common allergen. Consumers with milk allergies should not consume this product.
Product
Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe Springs, CA 90670 USA; UPC# 8 94042 00256 2
Category
Food
Distribution
1 state
HighFDA (Food)·F-0757-2025·2025-05-14
Heinen's Honey Roasted Peanuts Recalled for Undeclared Cashew Content
Trophy Nut Company is recalling Heinen's Honey Roasted Peanuts because the product is labeled as containing only peanuts but may contain undeclared cashews, a tree nut allergen.
Product
Heinen's Honey Roasted Peanuts, NET WT 8.25 OZ (234g), packaged in a composite can with plastic lid, 12 cans per case, Best If Used By: 10/01/2025 and Best By: 10/03/2025, UPC: 020601401877, Distributed By: Heinen's, Inc., Warrensville Hts., OH 44128
Category
Food
Distribution
2 states
HighFDA (Food)·F-0755-2025·2025-05-14
Lamb Weston frozen hashbrown patties recalled for plastic contamination
Lamb Weston Inc is recalling approximately 3,789 cases of frozen hashbrown patties due to the presence of plastic pieces measuring 1–8 mm in the product. No illnesses have been reported.
Product
Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW Formed Oval 6/3.5LB bags per case. GTIN*10044979922687. Made in USA.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1728-2025·2025-05-14
Artix MT Thrombectomy Device recalled for incorrect vessel range specification
Inari Medical is recalling 45 units of the Artix MT Thrombectomy Device (REF: 32-102, Lot 24100082) because labeling specifies an incorrect vessel range of 2.5-6 mm instead of 3-6 mm, which could increase radial force on arteries and cause vascular complications.
Product
Artix MT Thrombectomy Device, REF: 32-102
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V320000·2025-05-14
Winnebago Recalls 2023-2024 Commercial Vehicles Due to Step Bracket Defect
Winnebago is recalling 2023-2024 Commercial Vehicles because step mounting bolts may loosen, allowing steps to detach and increasing the risk of injury.
Product
WINNEBAGO — WINNEBAGO COMMERCIAL VEHICLE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1736-2025·2025-05-14
Introducer Needle REF NDL-107-04 Sterile Packaging Recall
Galt Medical Corporation recalls Introducer Needle REF NDL-107-04 due to potential open seals in sterile barrier packaging, which could compromise product sterility.
Product
Introducer Needle REF NDL-107-04 These needles are used for the percutaneous introduction of guidewires
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0754-2025·2025-05-14
Lamb Weston frozen hashbrown patties recalled for plastic contamination
Lamb Weston Item M7414 frozen hashbrown patties are recalled because approximately 1mm to 8mm pieces of plastic were found in the product. The affected cases were distributed in Arizona, Hawaii, and internationally.
Product
Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923820. Made in USA.
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0414-2025·2025-05-14
Testosterone Pellet 200 mg Recalled for Glass Particulate Matter
BSO LLC is recalling Testosterone Pellet 200 mg vials nationwide due to the presence of glass particles found in pellet vials. Patients should contact their healthcare provider.
Product
TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0124-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1735-2025·2025-05-14
Galt Medical Introducer Kit Coaxial Dilator recalled for packaging seal issue
Galt Medical Corporation is recalling certain Introducer Kit–Coaxial Dilator models due to potential open seals in sterile barrier packaging, which could compromise sterility.
Product
Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34, 00841268104792 KIT-002-35, 00841268104808 KIT-011-40, 00841268105553 KIT-011-62, 00841268105614 KIT-038-04, 00841268104556 KIT-039-03, 00841268104587 KIT-039-13, 00841268106055 KIT-081-02 / PS2-
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1733-2025·2025-05-14
B Braun Interventional ELITE HV Hemostasis Valve Introducer System Recall
Galt Medical Corporation is recalling the B Braun Interventional ELITE HV Hemostasis Valve Introducer System (Catalog Number 612802, Model BCL-100-04, Lot S25128171) due to a potential open seal in the sterile barrier packaging. The defect may compromise the sterility of the device.
Product
B Braun Interventional ELITE HV Hemostasis Valve Introducer System REF 612802 Model Number: BCL-100-04 The Elite HV¿ Introducer System is indicated for use in percutaneous procedures to introduce catheters and other intravascular devices into the vasculature.
Category
Medical Device
Distribution
Distributed nationwide

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7151–7175 of 89525