Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
USDA FSIS issued a public health alert for Costco Rotisserie Chicken Salad sold in Lynwood, Washington, due to a possible link to Salmonella illnesses.
Grand Design is recalling 2015-2017 Reflection trailers because the Federal Certification Label lists an incorrect Gross Axle Weight Rating, which could lead to loss of vehicle control.
Winnebago is recalling 2016-2017 travel trailers because weight labels list fresh water capacity in gallons instead of pounds, which may cause overloading.
Newmar is recalling 2017 King Aire, Essex, London Aire, and Mountain Aire motorhomes because a power steering pump defect may cause intermittent loss of steering assist.
Aqua Lung is recalling about 53,000 Powerline inflators because the inflation button can remain depressed, causing uncontrolled ascent and posing injury and drowning hazards.
Subaru is recalling 2017 Legacy and Outback vehicles because the knee guard bracket may not be properly attached, increasing injury risk in crashes.
GITI Tire is recalling specific Primewell, GT Radial, and Dextero tires that may develop sidewall cracks, potentially leading to air loss and tire failure.
Wildhorn Outfitters is recalling about 9,700 Outpost camping hammocks and suspension kits because cinch buckles can fail, posing a fall hazard.
Gleason is recalling about 120,000 Milwaukee hand trucks because plastic wheel rims can break, posing a laceration hazard.
Federico's Bakery is recalling Mexican Cookies because they contain undeclared milk as a sub-ingredient in butter.
Zyno Medical LLC is recalling 47,989 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients.
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels. The recall affects strips and kits distributed in the US and internationally.
Spacelabs Healthcare is recalling Xhibit Telemetry Receivers because the system may go offline or lock up, potentially failing to display alarms.
Pharmacy Plus, Inc. is recalling specific lots of DMSO 50% with Lidocaine 0.5% vials due to a lack of assurance of sterility.
Siemens Medical Solutions is recalling 103 PRIMUS linear accelerators to install a software patch addressing several safety issues.
Zyno Medical LLC is recalling 78,063 sterile administration sets due to a potential filter leaking defect. The sets are distributed nationwide for use with infusion pumps or gravity feed.
Dean Foods is recalling specific containers of Meadow Gold Heavy Whipping Cream because they were not pasteurized sufficiently. Consumers in Idaho, Oregon, Wyoming, and Utah should check their products.
Spiegelberg is recalling 22 Brain Pressure Monitoring System probes due to air chamber shrinkage that caused false high readings in the lower measuring range.
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.
Altec is recalling 219 model year 2014-2015 aerial devices because an improperly sized boom tip cover opening may allow contact with energized conductors, increasing injury risk.
Zyno Medical LLC is recalling 114,081 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients' vascular systems.
Spacelabs Healthcare is recalling Xhibit Central Stations because the telemetry system may go offline, lock up, or fail to display audio and visual alarms for asystole.
Daimler Trucks North America is recalling 2014-2017 Western Star 4900 and 5700 trucks because a seat belt mounting plate may have a hole that is too large, increasing injury risk in a crash.
Zyno Medical LLC is recalling 78,069 sterile administration sets because the filter may leak. The sets are used to administer fluids to patients.
Siemens Medical Solutions is recalling Syngo RT Therapist software to address several safety issues. The recall affects 103 linear accelerators nationwide.