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

2576–2600 of 36527

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 (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-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 (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-0405-2025·2025-05-14
Carboxymethylcellulose Sodium Ophthalmic Gel recalled for sterility concerns
BRS Analytical Services is recalling Carboxymethylcellulose Sodium Ophthalmic Gel 1% eye lubricant due to current Good Manufacturing Practice (cGMP) deviations and lack of assurance of sterility.
Product
Carboxymethylcellulose Sodium Ophthalmic Gel 1%, Carboxymethlycellulose Sodium 1% Eye Lubricant, Lubricant Eye Gel, Soothing Gel, Sterile, 0.5 FL OZ (15mL) per bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-066-15.
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-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 (Devices)·Z-1681-2025·2025-05-14
CADD-Solis Infusion Pump Thermal Damage Risk Recall
Smiths Medical is recalling CADD-Solis infusion pumps worldwide due to a potential for thermal damage. The affected pumps include multiple models and variants distributed in the US and internationally.
Product
CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, CE ENGLISH 1/EA, Model Number: 21-2111-0402-51; 2) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, YELLOW, CE ENGLISH 1/EA, Model Number: 21-2112-0402-51; 3) PUMP KIT, CADD-SOLIS, YELLOW, MODEL 21
Category
Medical Device
Distribution
Distributed nationwide
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-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 (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
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 (Devices)·Z-1679-2025·2025-05-14
Intraocular Lens Recalled Due to Toxic Anterior Segment Syndrome Reports
Bausch & Lomb has recalled multiple enVista intraocular lens models used in cataract surgery due to reports of toxic anterior segment syndrome (TASS) in the United States. TASS is an inflammatory reaction in the front of the eye following lens implantation.
Product
Intraocular lens. enVista Monofocal IOL, All models starting with EE; enVista Aspire IOL, All models starting with EA; enVista Monofocal Toric IOL, All models starting with ETE; enVista Aspire Toric IOL, All models starting with ETA;
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 (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
SevereNHTSA·25V255000·2025-05-12
Mercedes-Benz Recalls Vehicles With Incorrect Fuse Boxes From Prior Repair
Mercedes-Benz is recalling 443 vehicles that received an incorrect fuse box during a previous recall. The defect may cause loss of drive power, safety functions, or fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG EQS 53 4MATIC, AMG SL55 4MATIC+, AMG EQE 53 4MATIC, AMG SL63 4MATIC+
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V308000·2025-05-09
Ford Bronco lower control arms may detach; owners told not to drive
Ford is recalling certain 2024-2025 Bronco vehicles because front lower control arm fasteners may not be tightened, allowing the arm to detach. Owners are told not to drive.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V309000·2025-05-09
Ford Recalls 2025 F-150 Trucks for Steering Shaft Fastener Defect
Ford is recalling 2025 F-150 vehicles because lower steering shaft fasteners may detach, causing loss of steering control and increasing crash risk.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V314000·2025-05-09
Ford Expedition front brake lines may contact the air cleaner pipe
Ford is recalling certain 2022-2024 Expedition and Lincoln Navigator vehicles because front brake lines may contact the engine air cleaner outlet pipe and leak brake fluid.
Product
FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V316000·2025-05-09
Ford Explorer front subframe mounting bolts may be improperly tightened
Ford is recalling certain 2025 Explorer and Lincoln Aviator vehicles because a mounting bolt for the front subframe may have been tightened improperly. 206 units affected.
Product
LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V310000·2025-05-09
Ford Bronco upper control arm ball joint fasteners may be missing
Ford is recalling certain 2024-2025 Bronco and Ranger vehicles because the front upper control arm ball joint fastener may be missing or improperly tightened.
Product
FORD — FORD BRONCO, RANGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V300000·2025-05-08
Aston Martin Recalls 2024 Valkyrie Vehicles Due to Wiring Harness Risk
Aston Martin is recalling 2024 Valkyrie vehicles because incorrect screws may damage the wiring harness, potentially causing loss of critical functions and increasing crash risk.
Product
ASTON MARTIN — ASTON MARTIN VALKYRIE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E033000·2025-05-08
Chrysler Recalls Mopar Side Curtain Air Bags for Seam Defects
Chrysler is recalling specific Mopar side curtain air bags because improperly sealed seams may cause insufficient pressure retention, increasing the risk of ejection and injury during a crash.
Product
AIR BAGS:SIDE/WINDOW:CURTAIN recall
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25253·2025-05-08
Igloo 90 Qt. Rolling Coolers Recalled for Fingertip Amputation Risk
Igloo has expanded its recall of 90 Qt. Flip & Tow Rolling Coolers due to tow handle pinching hazards that can cause fingertip amputation or crushing injuries. About 130,000 additional coolers manufactured prior to January 2024 are affected.
Product
Igloo 90 Qt. Flip & Tow Rolling Coolers
Category
Consumer Product
Distribution
Distributed nationwide

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2576–2600 of 36527