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 the agency’s own highest classification or reported deaths or serious injuries, 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
GE HealthCare is recalling Revolution Ascend computed tomography systems due to a potential security vulnerability in the AW Server used with Edison Health Link-based CT Smart Subscription. 25 units are affected nationwide.
DJO, LLC is recalling the DonJoy IceMan CLASSIC3 cold therapy unit (Model 11-1424) due to a broken connector that may interrupt prescribed cold therapy treatment.
Swad Mango Flavored Masala Candy is being recalled because it contains undeclared Blue 1. The action covers 205 cases.
Jolife AB is recalling 153 LUCAS chest compression systems (Models 2, 3, and 3.1) due to incomplete service documentation. Service work performed on affected systems was not properly documented in service records.
DJO, LLC is recalling DONJOY ICEMAN CLASSIC CUBE cold therapy units due to broken connectors that may interrupt prescribed cold therapy. Approximately 596 units were distributed nationwide and in Canada.
Hologic is recalling certain 3DIMENSIONS MAMMOGRAPHY SYSTEM models due to internal bolts that may become loose, missing, or broken over time. The FDA classified this as a Class II recall.
Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging, which may compromise sterility.
Ascend Laboratories is recalling 17,304 bottles of Metoprolol Succinate Extended-Release 25 mg tablets (Lot #25140859, expiring Jan 2027) distributed nationwide because the tablets failed dissolution specifications, which may affect drug effectiveness.
Bolts and plastic parts of cable hose carriers on Philips Azurion X-ray systems may loosen or break during monitor movement or rotation, potentially causing the cable hose to become unsecured.
Endo USA, Inc. is recalling Buprenorphine Hydrochloride injection vials distributed nationwide due to the presence of particulate matter identified as Buprenorphine free base. The FDA classified this as a Class II recall.
Jerr-Dan is recalling XLP Carrier kits because reverse and brake light assemblies may be installed incorrectly, reducing vehicle visibility and increasing crash risk.
Hyundai is recalling certain 2025 Ioniq 5 and 2026 Ioniq 9 vehicles because the rear suspension fasteners may loosen and detach, which can cause a loss of vehicle control.
Hyundai is recalling certain 2025 and 2026 Tucson, Tucson Hybrid, Tucson PHEV, and Santa Cruz vehicles due to front camera software that may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes, increasing crash risk.
Endera is recalling 2025-2026 Shuttle buses because wheelchair retractors may fail to lock, increasing injury risk.
Keystone RV Company is recalling certain 2024–2026 recreational trailers because shock bolts may have been incorrectly tightened, which could cause loss of vehicle stability and increase crash risk.
Oshkosh is recalling 2025 NGDV electric vehicles because the high-voltage battery contactor may open unexpectedly in cold weather, causing a loss of drive power.
Tesla is recalling certain 2025 and 2026 Model Y vehicles because the certification label may not have been installed. Missing weight information on the label could lead to vehicle overloading and increase crash risk.
Altec is recalling specific aerial device vehicles because the ground-level emergency stop may fail to halt hydraulic functions in ePTO mode, increasing injury risk.
Generac and DR Power electric start pressure washers are recalled because the electronic start/stop button can malfunction and self-start the unit, creating a risk of serious injury or death from carbon monoxide poisoning in confined spaces. No injuries have been reported.
Minka Lighting Group is recalling about 170 Bardon Series Pendant Light Fixtures because the frame can detach from the downrod during installation, posing a risk of serious injury or death. One detachment has been reported with no injuries yet.
BRP US Inc. recalls about 2,820 Can-Am Outlander Pro and Max Pro ATVs with defective Speed Limiter Mode that can cause unexpected speed and acceleration, posing a risk of serious injury or death from crashes.
Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.
World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.
General Motors is recalling certain 2025–2026 GMC Yukon, Yukon XL, Chevrolet Tahoe, Suburban 1500, and Cadillac Escalade models with 24-inch wheels due to incorrectly installed front wheel hub bolts that may loosen or break, risking loss of vehicle control.
Guidecraft Kitchen Helper Towers are being recalled because the internal platform can loosen, become unstable, or detach, creating a fall hazard for young children. The company has received 11 reports of falls, including three injuries.