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.
Starcraft is recalling 50 model year 2014 Comet recreational vehicles because certification labels incorrectly identify tire load ranges, potentially leading to unsafe tire replacements.
Daimler Trucks North America is recalling 2014 Freightliner chassis because an incorrect speedometer calibration may display a lower speed than actual, increasing crash risk.
Riverside is recalling 2006-2014 travel trailers with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.
Yankee Candle is recalling Pine Berry candle rings because their synthetic foliage and berries are flammable, posing a fire hazard. No injuries have been reported.
Navistar is recalling 2,357 IC Bus school buses because seat belt buckles may fail to release, hindering emergency egress.
Browning is recalling approximately 4,300 Youth Buckmark Junior Hoodie Sweatshirts sold at Academy Sports+Outdoors due to a strangulation and entanglement hazard from neck drawstrings.
Red Wing Shoe Company is recalling approximately 114,000 pairs of steel toe work boots because the toe caps may fail to protect feet during impact.
Navistar is recalling 2014-2015 IC Bus CE and 2014 RECB transit buses because seat belt buckles may fail to release, potentially hindering emergency egress.
Edoche is recalling Cubetensils children's spoon and fork sets because the handles can detach, posing a choking hazard to infants.
Zimmer, Inc. is recalling specific sizes of the Trabecular Metal Total Ankle Tibial Base Component due to potential elevated levels of manufacturing residue.
Libbey Glass is recalling Bristol Valley cocktail glasses because they can break unexpectedly, posing a laceration hazard. One minor injury was reported.
IBA Dosimetry GmbH is recalling COMPASS SW Version 3.0 due to a software defect that causes erroneous dose statistics and DVHs.
Beckman Coulter is recalling LH 750 Hematology Analyzers because optical degradation may delay reporting results for specific blood cell counts.
Zimmer, Inc. is recalling specific Total Ankle Talar Components due to potential elevated levels of manufacturing residue on the implants.
Arrow International Inc is recalling Transradial Artery Access products because introducer needles may be occluded, posing a risk of delayed treatment or adverse events.
Price Chopper Supermarkets is recalling 8-inch and 10-inch Coconut Custard Pies because they lack an ingredient statement and contain undeclared eggs, tree nuts, milk, wheat, and soy.
GE Healthcare is recalling specific patient monitors because they may apply an incorrect ECG filter setting if impedance respiration is enabled at startup.
Spartan Motors is recalling one 2006 Utilimaster truck body because a specific door lock can jam, potentially trapping occupants inside the cargo area.
Maquet Cardiovascular is recalling 12,259 units of the Vasoview Hemopro Endoscopic Vessel Harvesting System due to complaints that the device self-activates or overheats.
Zero Motorcycles is recalling 667 model year 2012-2013 motorcycles because a firmware fault may shut off power to the motor, increasing crash risk.
Zimmer, Inc. is recalling five NexGen knee instruments to prevent their inadvertent use during surgery, which could cause delays.
Trumpf Medical Systems is recalling 287 Helion S and H300 exam lights because a plastic joint may fail due to fatigue after seven years of use.
Hospira is recalling 1L Receptal Canisters because the canister and liner may not seat properly, preventing the creation of necessary suction.
Zimmer, Inc. is expanding a recall of NexGen Porous Patella Drill Guides to prevent inadvertent use during surgery, which could cause delays.
Centurion Medical Products is recalling sterile rubber bands that are labeled as both latex-free and containing natural rubber latex, posing a risk to users with latex allergies.