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.
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.
Minimum severity
iLet Ace Pump Kits are being recalled because active status bar icons on the lock and passcode screens allow those screens to be bypassed, permitting unauthorized access.
Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP ampules are being recalled for lack of assurance of sterility. The action covers 3,260,170 ampules.
Cytal Wound Matrix 2-Layer 10x15 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 452 units are affected.
HydroPeptide Clear Alliance Serum, a 2.5% benzoyl peroxide product, is being recalled because of chemical contamination from the presence of benzene. 9,850 bottles are affected.
Lidocaine HCl Injection, USP 1% in 5 mL single dose vials manufactured by Huons is being recalled for lack of assurance of sterility. All lots within expiry are affected.
SLMD Benzoyl Peroxide Acne Lotion, 2.5% benzoyl peroxide, is being recalled because of chemical contamination from the presence of benzene. 2,500 bottles are affected.
Philips is recalling the Spectral CT on Rails after identifying three software issues affecting gantry movement, a confirmation prompt and head area planning. Three systems are affected.
Cytal Wound Matrix 2-Layer 5x5 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 148 units are affected.
International Medication Systems is recalling one lot of Epinephrine Injection, USP, 1 mg/10 mL, citing lack of assurance of sterility. 81,520 units are affected.
Gentuity is issuing a correction for HF-OCT Imaging Systems because frames may repeat during pullback with Vis-Rx catheters, affecting longitudinal length measurements.
Major Pharmaceuticals is recalling one lot of Memantine Hydrochloride Extended-Release Capsules, 7 mg, after the product failed dissolution specifications.
Tesla is recalling certain 2024-2026 Cybertruck vehicles with 18-inch steel wheels because brake rotor stud holes may crack and allow the stud to separate from the wheel hub.
Forest River is recalling 2026-2027 East to West recreational vehicles because the fender may contact and damage the rear tire, increasing crash risk.
Mitsubishi is recalling certain Outlander and Outlander PHEV vehicles because the liftgate gas spring cylinders may corrode and lose pressure, risking rupture or a falling liftgate.
Hexagon Purus is recalling 2025-2026 Tern RC8 vehicles because a software error may cause the digital display to show incorrect air brake pressure, potentially failing to alert drivers to actual brake issues.
Q'Straint is recalling QRT-3 wheelchair retractors that may fail to lock, preventing proper wheelchair securement and increasing injury risk during transit.
Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 buses because the driver seat belt anchor may have inadequate hardware, increasing injury risk in a crash.
Hyundai is recalling certain 2025 and 2026 models including Tucson Hybrid, Tucson, Elantra, and Elantra N due to misassembled B-pillar impact sensors that may delay air bag deployment in a crash.
Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 school buses because the driver seat belt anchor may have inadequate hardware.
Goodyear is recalling specific Eagle F1 Supersport tires because the tread may separate, increasing the risk of a crash. Owners should contact Goodyear for a free replacement or refund.
Jaguar Land Rover is recalling certain mild-hybrid vehicles because the DC-DC converter can fail due to an internal fault, causing a loss of drive power. 170,169 vehicles are affected.
Altec is recalling 2025-2026 Digger Derrick and Aerial Device vehicles because improperly installed front-end radar may cause unexpected brake activation, increasing crash risk.
Blue Bird is recalling 2026 All American transit buses because improperly tightened wiper fasteners may cause wipers to fail, reducing visibility and increasing crash risk.
Blue Bird is recalling 2026-2027 All American school buses because improperly tightened wiper fasteners may cause wipers to fail, reducing visibility and increasing crash risk.
Chrysler is recalling specific Mopar engines where internal debris may cause failure, leading to loss of drive power or engine compartment fire.