Hazard
293 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all structural defect recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
The port weld in ICU Medical ChemosafeLock connecters (REF: KL-FNU3) may separate or break during use, potentially causing drug leakage. Approximately 134,700 units have been distributed worldwide.
Biomet is recalling one lot of ZipTight AC Joint Implants due to a potential missing slotted button assembly that could compromise fixation. The recalled lot contains 98 units.
Abbott is recalling TactiFlex Sensor Enabled Ablation Catheters due to tip detachment events occurring during removal from packaging. Limited units distributed worldwide are affected.
YGJT baby loungers sold on SHEIN from June to August 2025 violate mandatory infant sleep safety standards. The sides are too low and openings are too wide, creating fall and entrapment hazards for infants.
North American Rescue is recalling 552 JETT devices used to control bleeding in limbs due to a potential manufacturing defect that may compromise device performance during use.
ORTOMA AB recalls Ortoma Inserter Adapter OTD hip surgical devices due to weld breakage between the pin and inserter holder. The defect affects 261 devices distributed in Florida and internationally.
Maquet Cardiovascular is recalling the Vasoview Hemopro 3 endoscopic vessel harvesting system due to out-of-box mechanical failures including deformed jaws and heater wire defects discovered during the limited launch phase.
Stryker Communications is recalling Chromophare Surgical Light Systems due to stress lines in the powder coating that may cause chipping. 40 units were distributed nationwide.
Medtronic is recalling 34,549 DLP Left Heart Vent Catheters (Model 12113) because the catheters may not retain their shape. The defect affects devices distributed worldwide and could compromise catheter function during cardiac surgery.
Medtronic is recalling DLP Left Heart Vent Catheters (Model 12110) because they may not retain their shape during use. This defect could affect device function in cardiac surgical procedures.
Ford is recalling certain 2024-2025 Ranger and Bronco vehicles because the front upper control arm ball joint fastener may be missing or improperly tightened, potentially allowing the control arm to detach and cause loss of steering control.
Ford is recalling 206 model-year 2025 Explorer and Aviator vehicles with potentially improperly tightened front subframe bolts that may compromise crash safety. Contact Ford Customer Service at 1-866-436-7332 for free inspection and repair.
THOR is recalling 55 NovoTHOR XL heating devices due to potential failure of the welded nut securing the gas strut. If the nut shears, the canopy may become difficult to lift.
The Atlantis IO FLO-S dental prosthetics device has a defect preventing proper thread engagement with dental implants. Threads engage only about 2 rotations instead of the required 5, resulting in approximately 1mm less depth of engagement.
THOR NovoTHOR phototherapy devices (Model S2188) may have a failed welded nut causing the canopy gas strut to detach, making the canopy difficult to lift. Eighty units have been recalled.
DT Swiss has recalled about 6,000 Carbon Fiber Road Wheels due to a defect that can compromise structural integrity and cause crashes. No injuries have been reported.
Apollo is recalling approximately 790 Model Year 2024 electric scooters because the stem weld can crack and break during use, creating a fall hazard. Reports include 10 instances of stem cracking, 4 riders falling, and one injury.
Edwards Lifesciences is recalling OptiSite Arterial Cannulas (Model OPTI18) due to exposed wire protruding from the device body. Approximately 13,240 units distributed worldwide are affected.
Medtronic is recalling 3 units of the O-arm O2 Imaging System (mobile X-ray equipment) in IN, MN, and MS due to potential damage to a mechanical component supporting the gantry during manufacturing.
Grand Design is recalling 2019-2024 Solitude fifth wheel trailers because step tread joints may be unsupported, causing treads to break and increasing injury risk. Dealers will reinforce step treads with metal brackets at no cost.
Mercedes-Benz is recalling certain 2025 E 350, E 350 4MATIC, E 450 4MATIC, and E 450 4MATIC station wagon models due to an improperly welded bracket. The defect may cause loss of vehicle control and increase crash risk.
Mercedes-Benz USA is recalling certain 2023-2025 GLC 300 models and related SUVs with panoramic sunroofs due to insufficient C-pillar impact protection. The defect fails federal safety standards and increases injury risk.
ZHORANGE portable bassinets sold on Amazon from November 2024 through April 2025 violate federal safety standards because the sides are too low and there is no stand, creating a fall hazard for infants. No injuries have been reported.
The FDA is recalling the Cardiohelp System HKH 8820 Wall Holder mounting bracket because it does not comply with safety standards and has the potential to detach during interhospital transport.
Waldemar Link is recalling Tibial Augment medical devices because preassembled Femoral Augment screws are missing their threads, preventing proper fixation. The recall affects 1771 units distributed nationwide.