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.
Gudook Adult Bike Helmets (model KY-055, batch 202503, March 2025 manufacture) violate mandatory safety standards and fail to protect users in a crash, posing a serious risk of head injury or death. About 520 units sold on Amazon from May 2025 through February 2026.
TOMY International is recalling Boon NURSH 8 oz Reusable Baby Bottles because the hard plastic outer shell can bubble or peel, creating loose plastic pieces that pose a choking hazard to young children. No injuries have been reported.
GE HealthCare is recalling trade-in CARESCAPE Telemetry Servers because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
Philips Allura Xper interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.
Wawa Beverage Company is recalling Wawa Iced Tea Lemon 16 oz Pint plastic bottles because they contain undeclared milk.
GE HealthCare ApexPro v6.0 eDelivery Software is being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
GE HealthCare CARESCAPE Telemetry Servers ARK-2250L are being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
Jayco is recalling 2026 Melbourne Prestige and Entegra Qwest recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.
Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.
Halyard Purezero Ultraviolet Nitrile Exam Gloves are being recalled because they failed to meet specifications for chemical permeation performance. 452,500 units are affected.
Medline EYE TRAY-LF kits are being recalled because they contain Cardinal Health syringes packaged as 1 mL tuberculin syringes but which are actually U-100 insulin syringes.
Fly By Jing Creamy Sesame Noodles are being recalled because possible cross-contamination resulted in an undeclared peanut allergen. 3,419 cases are affected.
Jayco is recalling 2026 Entegra and Jayco recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.
GE HealthCare is recalling CARESCAPE Telemetry Server V5 ATO models because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.
GE HealthCare IOU assemblies for the ARK2250 CARESCAPE Telemetry Server are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of monitoring.
HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.
GE HealthCare ApexPro v5.0 Software Disaster Recovery USB Kits are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of ECG and SpO2 monitoring.
Braun is recalling 2026 Ram ProMaster vehicles with specific wheelchair seat belts that may have incompatible connectors and fail to restrain occupants.
Kia is recalling 2027 Telluride and Telluride Hybrid vehicles because the driver seat belt may fail to extend, increasing injury risk in a crash.
Nova Bus is recalling LFS and LFS Artic transit buses because the low brake air pressure warning light may fail to illuminate when the engine is off, increasing crash risk.
Chrysler is recalling 2023-2026 Pacifica and Voyager vehicles because a spring may prevent air bags from deploying, increasing injury risk.
Synear Foods is recalling about 71,603 pounds of frozen pork and crab soup dumplings because the products were formulated with peanut oil but peanuts were not declared on the label.
Mercedes-Benz USA is recalling 2026 GLS, GLE, and Maybach models due to rear seat belt bolts that may not be properly tightened, reducing restraint effectiveness in a crash.
Forest River is recalling certain 2024-2026 Wildwood and Salem travel trailers because the fireplace outlet may have incorrect wiring, increasing the risk of a fire.
Daoen Inc. is recalling Zen Fidget Magnetic Ball Sets because the loose high-powered magnets can be swallowed by children, causing intestinal perforation, blockage, or death. No injuries have been reported.