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.
Eclipse is recalling 2020-2021 Attitude, Stellar, and Iconic trailers because a stove bolt may be overtightened, damaging the seal and causing a gas leak.
Shyft Group is recalling certain 2021–2022 Spartan K2 RV Chassis vehicles with Cummins L9 Diesel Engines due to fuel leaks from pressurized hoses. The leak may increase fire risk if an ignition source is present.
Marion Body Works is recalling 2009-2021 Spartan Fire Gladiator and MetroStar emergency vehicles because a corroded solenoid may cause loss of water pressure.
Volkswagen is recalling certain 2021 Audi E-Tron models due to improperly welded brake boosters that may separate, reducing braking assistance and stability control.
Top Notch Jerky LLC is recalling 107 pounds of beef jerky because the product contains anchovies, a known allergen, that are not listed on the label.
Ricon is recalling Baylift Wheelchair Lifts because the outer barrier may fail to withstand maximum force, increasing injury risk.
Rosenbauer America is recalling 2012-2016 Warrior and Commander vehicles because incorrect weight and tire pressure information on the certification label may lead to underinflated tires.
Polaris is recalling about 1,700 Model Year 2021 RZR Pro XP and RZR Pro XP 4 recreational off-road vehicles because a raised edge on the turbocharger casting can cause an oil leak and fire hazard.
Continental Automotive Systems is recalling PSAT side crash pressure sensors that may loosen due to improper mold cleaning, potentially delaying side air bag deployment.
BRP is recalling about 34,400 model years 2020 and 2021 Can-Am Defender HD10 side-by-side vehicles because the CVT air intake can become obstructed with snow, causing the drive belt to overheat and break and creating a fire hazard. BRP has received three reports of fires but no injuries.
Polaris is recalling Model Year 2021 GENERAL 1000, GENERAL 4 1000, GENERAL XP 1000, and GENERAL XP 4 1000 recreational off-highway vehicles because a weld between the brake pedal pivot bracket and EPS mounting bracket can separate, resulting in loss of brake function.
Altec is recalling 2016-2021 Digger Derricks because the pole guide joystick can be inadvertently moved by the operator's forearm, posing an injury risk.
Heartland is recalling certain 2021 Mallard and North Trail recreational trailers with improperly routed refrigerator roof vents. The defect risks fire and carbon monoxide poisoning.
Canon Medical System is recalling Canon Vantage Galan 3T MRI systems due to a component that does not meet flame retardancy standards, which could result in smoke or fire. The recall affects units distributed nationwide.
RanD S.r.l. is recalling Hang&Go hyperthermic perfusion kits due to a sterilization process failure that may have left some units non-sterile. The recall affects 72 kits distributed to Florida, Illinois, Tennessee, and Wisconsin.
Canon Medical's Toshiba Vantage Tiitan 1.5T MRI systems are being recalled due to a component that does not meet flame retardancy standards. The defect could result in smoke or fire. Affected units were distributed nationwide.
GE Healthcare's Discovery MR450 1.5T MRI system may inadvertently change patient orientation when users click the wrong button, resulting in flipped or incorrectly annotated images that could affect diagnostic accuracy.
Bazzini LLC is recalling Trader Joe's Dark Chocolate Almond Butter Cups (1.4 oz, 2-cup packs) due to potential undeclared peanut allergen. Affected consumers should not consume the product if they have a peanut allergy.
Axonics is recalling BULKAMID urethral bulking system needles that may not have been adequately sterilized despite sterile labeling. Unsterilized surgical needles pose infection risk.
GE Healthcare SIGNA Voyager MRI systems may display flipped or incorrectly annotated diagnostic images due to button confusion on the system interface. 541 devices are affected worldwide.
Central hole cover plugs on EcoFit cementless acetabular cups may come loose during surgical implantation, potentially extending operation time or requiring revision surgery. Fifty-one units in Florida and Texas are affected.
Owen Mumford USA is recalling Unifine Pentips Plus pen needles because two cases of 4mm needles were mistakenly packaged as 8mm needles, which could result in patients receiving incorrect needle sizes for their insulin pens.
GE Healthcare recalls 91 SIGNA HDxt MRI systems worldwide. The Patient Orientation button may be accidentally clicked instead of Save RX, potentially causing diagnostic images to be incorrectly oriented or flipped.
Arrow International is recalling its Temporary Pacing Catheter/Introducer Kit because it was marketed without required FDA 510K clearance. Approximately 15 units were distributed in multiple U.S. states.
GE Healthcare recalls 460 SIGNA Pioneer MRI scanners worldwide due to a control panel button design flaw. Patient Orientation button may be accidentally clicked instead of Save RX, potentially resulting in incorrect image annotation or orientation.