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.
Daimler Trucks North America is recalling 2017-2018 Freightliner Cascadia vehicles because brake lights may stay on after the pedal is released, increasing crash risk.
Chrysler is recalling 2019 Jeep Cherokee vehicles with 2.4L engines because improper transmission calibration may cause a stall, increasing crash risk.
Forest River is recalling 2019 Impression fifth wheels because side marker lights are misplaced, reducing visibility and increasing crash risk.
Forest River is recalling specific 2017-2019 motorhomes because a damaged rear module may cause marker, brake, or turn signal lights to stop working.
Hydrolevel is recalling HydroStat Model 3000 boiler controllers for Slant/Fin boilers because a malfunction can cause overheating and fire. No injuries or property damage have been reported.
Vista Railing Systems is recalling ProBuilt aluminum deck railing posts because they can separate from the base, posing a fall hazard. No injuries have been reported.
Charles Machine is recalling 2018 Ditch Witch trailers with vacuum excavators because the jib boom can become loose and swing outside the trailer while being towed.
Kikkerland is recalling wireless charger bedside pockets because they can overheat, posing fire and burn hazards. Three reports of smoke have been received, with no injuries reported.
Sarap Asian Fusion is recalling Matcha Chocolate cookies because they contain undeclared wheat and soy lecithin. The cookies were sold online to customers in multiple states.
Sterilmed, Inc. is recalling 218 reprocessed Agilis Steerable Introducers because they may not meet endotoxin requirements. The devices were distributed in California, Colorado, Minnesota, and Washington.
Great Dane is recalling 2019 Champion Composite Plate dry freight trailers because they may have insufficient reflective tape, reducing visibility and increasing crash risk.
Albertsons Inc is recalling Signature Reserve Bourbon Maple Blondie Ice Cream due to undeclared tree nuts. The product was distributed in Oregon and Washington.
Orthosensor, Inc. is recalling 41 VERASENSE sensors for Zimmer Biomet Persona CR E-F/3-11 Left knees because fluid was reported inside the posterior lateral corner after surgery.
Medline Industries is recalling Unna Boot Compression Wraps because sporadic reports identified common mold on certain lots.
Bayer is recalling Codan Filters used in IV administration sets because the dust cap may generate particulate that enters the fluid path.
Neomed Inc is recalling NeoMed Enteral Feeding Tubes because the tethered plug may inadvertently open after closure, potentially compromising the device's seal.
Alkano Chemicals, Inc. is recalling 8 kg of Thyroid Powder, Lot # 170501, due to inconsistent levels of active ingredients levothyroxine and liothyronine.
Sarap Asian Fusion is recalling Black Sesame White Chocolate cookies due to undeclared wheat, soy lecithin, and milk.
Orthosensor, Inc. is recalling 68 VERASENSE sensors for Zimmer Biomet Persona CR G-H/7-12 Right because fluid was reported inside the posterior lateral corner post-surgery.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because they may dispense insufficient sample volume without suppressing potentially incorrect results.
Orthosensor, Inc. is recalling 36 VERASENSE sensors for Zimmer Biomet Persona CR C-D/3-9 Right knees because fluid was reported inside the posterior lateral corner post-surgery.
CooperSurgical is recalling Colpo-Pneumo Occluder devices because the sterile pouch seal may be compromised, increasing the risk of infection.
Sarap Asian Fusion is recalling Miso Milo Chocolate cookies because they contain undeclared wheat and soy lecithin. The cookies were sold online to customers in multiple states.
Orthosensor, Inc. is recalling 84 VERASENSE sensors for Zimmer Biomet Persona CR G-H/7-12 Left because fluid was reported inside the posterior lateral corner post-surgery.
Orthosensor, Inc. is recalling 56 VERASENSE sensors for Zimmer Biomet Persona CR C-D/3-9 Left because some were reported to have fluid inside the posterior lateral corner post-surgery.