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.
Spartan Fire is recalling one 2019 Gladiator firefighting vehicle because a disabled sleep mode on the wireless remote controller causes batteries to discharge faster than normal.
Nova Bus is recalling 2016-2019 LFS buses because the rear door obstruction safety mechanism may fail, increasing injury risk.
Motor Coach Industries is recalling 1,067 buses because debris or water may cause excessive alternator voltage, leading to engine shutdown and increased crash risk.
Gillig LLC is recalling 6,353 aftermarket rear suspension lower control rods due to a risk of fatigue failure that could reduce vehicle handling and stability.
Keystone RV Company is recalling 428 model-year 2020 trailers because window glass may detach while moving, creating a projectile hazard.
KYMCO is recalling 2018-2019 Like 150i scooters because excessive grease on the ABS sensor may cause deterioration and system failure, increasing crash risk.
Coach and Equipment is recalling 2019-2020 Phoenix mini-buses because seat belt retractors may not secure occupants properly, increasing injury risk in crashes.
Bonnsu is recalling Miniware teething spoons because they can break in an infant's mouth, posing a choking hazard. One injury report has been received.
Lode-King is recalling one 2021 Prestige SDG semi-trailer because the load rating decal exceeds the frame's strength capability, increasing crash risk if overloaded.
Davina Wellness is recalling wintergreen essential oils because the packaging is not child-resistant, posing a risk of poisoning to young children.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.
The FDA is recalling 12,610 units of the Multifire VersaTrack Auto Suture Hernia Stapler because a manufacturing error may prevent staples from advancing properly.
Zilks Foods is recalling Plucker's Wing Bar World Famous Wing Sauce Spicy Mandarin due to potential undeclared milk and wheat allergens.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.
Baxter Healthcare is recalling Gambro Cartridge Blood Transport Systems due to a potential disconnection of the tubing set. The recall covers 53,895 units distributed worldwide.
Med Tec Inc is recalling Type S Extensions used for patient positioning due to a risk of disengagement during repositioning, which could cause a patient fall.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.
Cell-nique Corp is recalling Cherrybrook Kitchen Sugar Cookie Mix because the product is labeled gluten-free and wheat-free but contains wheat.
American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.
American Contract Systems is recalling sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.
Beckman Coulter is recalling Access Free T4 Thyroxine assays because biotin can cause significant result bias, potentially affecting patient care.
Insulet is recalling 400 Omnipod DASH insulin systems because the Bolus Calculator may fail to subtract insulin on board correctly after two months of use.
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.