Hazard
97 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 97 fluid leak recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 35 (36%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all fluid leak 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.
Harley-Davidson is recalling 45,589 2017 motorcycles because an improperly installed clamp may cause the engine oil cooler line to detach, increasing crash risk.
Thor Motor Coach is recalling 2016-2017 Venetian and Tuscany motorhomes because a power steering hose may rub against the starter motor, causing electrical arcing and fluid leaks that increase fire risk.
Elcam Medical, Inc. is recalling 810 units of Minimal Residual Volume Luer-activated Swabable-stockcock devices found to have punctures.
Nissan is recalling 2013-2014 Murano vehicles because a power steering hose clamp may fail, causing fluid leaks that could ignite near hot engine parts.
Terumo is recalling Sarns Centrifugal Pumps because cracks in the housing can cause fluid leaks during cardiac procedures. No patient injuries have been reported.
Baxter Healthcare is recalling Phoenix Dialysis Machine Preventive Maintenance Kits due to incorrect silicone connectors that may cause fluid leaks.
Baxter Healthcare is recalling Phoenix Dialysis Machine Preventive Maintenance Kits due to incorrect silicone connectors that may cause fluid leaks during dialysis.
Reshape Medical is recalling 114 units of the Integrated Dual Balloon System Gen 1 because distillation fluid may leak during inflation.
Ford is recalling 2013-2014 F-150 trucks with 3.5L engines because a seal defect may cause brake fluid leakage and loss of front brake function.
Siemens is recalling 1,757 Artis zee/zeego angiographic X-ray systems because a possible leak in the cooling system could allow fluids to seep into the equipment cabinet.
Xeridiem is recalling 36 EndoVive 3s Low Profile Balloon Kits because the feeding valve may close inconsistently, allowing fluid to leak.
Kia is recalling 2011 Fortes because a defective transmission cooler hose may leak fluid, potentially causing the vehicle to stop moving and increasing crash risk.
Chrysler is recalling 2015 Jeep Compass and Patriot vehicles because a power steering hose clamp may be installed incorrectly, increasing the risk of a fire.
Stryker is recalling Neptune 2 Waste Management System Docking Stations because a defective component may cause fluid leaks during use.
Subaru is recalling 2015-2016 Legacy and Outback vehicles because a deformed seal cap may allow transmission oil to leak onto the exhaust pipe, creating a fire risk.
Integra LifeSciences is recalling Camino Intracranial Pressure Monitoring Catheters because incorrect assembly may allow cerebrospinal fluid or blood to leak.
ICU Medical is recalling specific arterial monitoring kits because a component connection may crack, causing a fluid leak.
ICU Medical is recalling 20 units of Transpac IV Trifurcated Monitoring Kits because a component connection may crack, causing a fluid leak.
ICU Medical is recalling 40 units of Trifurcated Transpac IT Monitoring Kits because a component connection may crack and cause a fluid leak.
ICU Medical is recalling 100 units of Transpac IT arterial monitoring kits because a component connection may crack and cause a fluid leak.
ICU Medical is recalling specific arterial monitoring kits because a component connection may crack, causing a fluid leak.
ICU Medical is recalling 200 arterial monitoring kits because a component connection may crack, causing a fluid leak.
ICU Medical is recalling 50 units of Transpac arterial monitoring kits because a component connection may crack and cause a fluid leak.
ICU Medical is recalling specific arterial monitoring kits because a component connection may crack, causing a fluid leak.
ICU Medical is recalling 60 units of Trifurcated Transpac IV Monitoring Kits because a component connection may crack and cause a fluid leak.