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.
Sauder Woodworking is recalling about 3,100 counter-height bar stools because the legs can become unstable, posing a fall hazard. No injuries have been reported.
Siemens Medical Solutions is recalling Sensis and Sensis Vibe Hemo systems due to Windows Service Permission configuration risks that could expose sensitive information or allow data manipulation.
Siemens Healthcare Diagnostics is recalling BCS XP Systems due to a potential risk of Emicizumab carryover on patient samples.
Biotronik is recalling eight Intica Neo 7 HF-T implantable defibrillators due to a potential for premature battery depletion.
AngioDynamics is recalling specific lots of Smart Port CT-Implantable Port kits due to potential compromised sterility. The recall affects 267 kits distributed nationwide.
Forest River is recalling 2021 Coachmen Catalina travel trailers because an incorrectly gauged battery wire may melt and cause a fire.
REV Ambulance Group Orlando is recalling 2019-2021 Type I and IX ambulances because LCD displays may lock up, potentially delaying emergency efforts.
Rosenbauer America is recalling specific fire trucks because rear lights may be too bright, potentially blinding other drivers and increasing crash risk.
Gillig is recalling 229 CNG-powered buses because insufficient roof door overlap may allow accidental opening, increasing crash risk.
Kawasaki is recalling about 70 2021 BRUTE FORCE 750 ATVs because loose fuel pump bolts can cause fuel leaks and fire. No injuries have been reported.
Kawasaki is recalling about 100 2021 Teryx off-highway utility vehicles because loose fuel pump bolts can cause fuel leaks and fire. No injuries have been reported.
HME is recalling 2013-2021 AF1, 1871, and SFO vehicles because cracked wiring insulation may cause aerial controls to fail, creating a shock risk.
Navistar is recalling certain 2019-2021 International LT and RH trucks due to wrist pin cracks that can cause connecting rod failure and engine stalls. Affected owners should contact their dealer for free repair.
Chrysler is recalling 2020-2021 Dodge Durango vehicles because the side curtain air bag fastener may be loose or missing. A loose fastener could cause incorrect air bag deployment, increasing injury risk.
Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because documents may list the wrong weight rating, potentially leading to overloading and crashes.
YYBA is recalling Welmate Lidocaine Numbing Cream because the packaging is not child-resistant, posing a risk of poisoning to young children.
Nissan is recalling 2021 Rogue vehicles because the rear brake calipers may be missing an internal bushing, causing brake fluid to leak and reducing braking performance, increasing the risk of a crash.
HME is recalling 2016-2021 AF1 and 1871 vehicles because the self-leveling function may malfunction, causing the aerial bucket to move unexpectedly and increasing injury risk.
Siemens Healthcare is recalling 132 ADVIA 2120 hematology analyzers because a software defect may cause sample identification mismatches with 14-character barcodes.
Volkswagen is recalling 2021 Arteon vehicles because incorrectly calibrated tire pressure sensors may fail to detect low air pressure, increasing crash risk.
BRAV USA is recalling Swix Focus Down Jackets Jr. because hood and waist drawstrings pose strangulation and entrapment risks to children.
Siemens is recalling 187 ADVIA 2120i Dual Aspirate Autosamplers due to a potential sample identification mismatch with 14-character barcodes.
Akron Brass is recalling Weldon V-Mux Vista IV LCD displays used in emergency vehicles due to a defect that may cause the screen to lock up or become nonfunctional.
Metal Ware is recalling NESCO Coffee Bean Roasters because they can overheat and cause fires. Consumers should stop using the units and contact the company for a refund.
Siemens is recalling 7 ADVIA 2120 automated hematology analyzers due to a potential sample identification mismatch with 14-character barcodes.