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.
About 68,000 Trek and Electra bicycles with coaster brakes, plus replacement rear wheels, are being recalled because the coaster brakes can fail to engage.
Forest River Bus is recalling 2025-2026 transit buses because wheelchair restraints may fail to lock, increasing injury risk.
Honda is recalling 256,603 model year 2023-2025 Accord Hybrid vehicles because a software error may reset the integrated control module CPU while driving, causing a loss of drive power.
About 380 Bettina Doll Sets with Magic Light Unicorn are being recalled because the unicorn's battery compartment lets children easily access button cell batteries.
Forest River Bus is recalling certain 2025-2027 school buses because wheelchair restraints may fail to lock, increasing injury risk.
International Motors is recalling 142 model year 2023-2027 IC Bus CESB school buses because the bus may exceed its Gross Vehicle Weight Rating when fully occupied with full tanks.
About 32,600 Great Lakes Select button cell and coin battery packs are being recalled because they lack the child-resistant packaging and warning labels required under Reese's Law.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 13 cm, over a potential issue with the seal integrity of the header bag packaging.
AquaStar is recalling 3,600 cases of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp because the shrimp may be contaminated with Cesium-137.
Dr. Praeger's Sensible Foods is recalling 648 master cases of California Veggie Burgers because the product was made on equipment that tested positive for Listeria.
Ice Cream Factory is recalling 255 ten-pound boxes of Bakery Graham Pieces after aluminum foil and packaging fragments were found in a brown sugar ingredient.
AquaStar is recalling 2,916 cases of Publix Large Shrimp Peeled & Deveined Tail On 31/40 because the shrimp may be contaminated with Cesium-137.
Que Rikura's Products is recalling 31,953 cases of 4 oz frozen coconut bars distributed in Florida because sulfites are undeclared on the product label.
AquaStar is recalling 5,220 cases of AquaStar Raw Peeled Tail-on Shrimp Skewers because the shrimp may be contaminated with Cesium-137.
AquaStar is recalling 7,200 cases of AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, sold at WinCo, because the shrimp may be contaminated with Cesium-137.
Zimmer is recalling 72 Dual Mobility Vivacit-E bearings labelled Size F 44 mm because the implant inside the package is a Size G 46 mm, and the reverse also occurred.
Eagle Spice and Extract is recalling 2,476 units of Eagle Spice Ground Ginger 16 oz because the product contains elevated levels of lead.
Teva Pharmaceuticals USA is recalling 4,680 cartons of Amoxicillin and Clavulanate Potassium for Oral Suspension 200 mg/28.5 mg per 5 mL because the clavulanate component is subpotent.
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
TBC Distribution is recalling 5,598 units of Lucky Foods Cinnamon Powder 40g because the product may contain elevated levels of lead.
AquaStar is recalling 9,900 cases of Best Yet Frozen Raw EZ-Peel White Shrimp across multiple counts because the shrimp may be contaminated with Cesium-137.
Beckman Coulter is recalling 80 UniCel DxI 600 analyzers because defective gantry sub-components can cause a z-axis motion error that halts the analyzer and delays results.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 16 cm, over a potential issue with the seal integrity of the header bag packaging.
AquaStar is recalling 1,458 cases of Publix Extra Large Shrimp Easy to Peel Deveined 21/25 because the shrimp may be contaminated with Cesium-137.
Elekta is recalling 338 Leksell Vantage Stereotactic System components because paint flakes from the engravings may separate and could inadvertently enter the wound.