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.
Collins Bus Corporation is recalling 2018-2019 TL400, TL408, TH400, and TH408 school buses that may lack rear backup cameras, increasing crash risk.
Subaru is recalling 2017-2019 Impreza and 2018-2019 Crosstrek vehicles because a software defect may cause the engine to stall while driving, increasing crash risk.
Vac-Tron is recalling 2015-2019 LP 873 SD heavy trailers because they may sway while being towed, increasing the risk of a crash.
Polaris is recalling 2015-2019 Slingshot motorcycles because excessive electrical current may damage battery fuse terminals, potentially causing loss of lighting or power steering and increasing crash risk.
Cummins is recalling 104 PowerDrive EV Vehicle Control Units because a software error may cause unexpected vehicle movement during slow driving.
Honda is recalling Genuine Accessory Rear Carriers for 2019-2020 Monkey motorcycles because they may fail under load, posing a crash risk.
Dorel is recalling 28,800 Babidéal Storm Booster Car Seats sold at Family Dollar because the fabric cover may lack required safety warnings, increasing crash injury risk.
Subaru is recalling 2017 Impreza vehicles because a defective PCV valve may break apart and enter the engine, causing a loss of power while driving.
Subaru is recalling 2017-2018 Impreza and 2018 Crosstrek vehicles because the PCV valve may break apart, potentially causing a loss of power while driving.
Conformis, Inc. is recalling two iTotal Hip Replacement femoral stems because sizes 13 and 15 were packed in each other's packaging.
Forest River is recalling 2020 Sunseeker, Freelander, and Leprechaun vehicles because the seatbelt warning light may not illuminate, increasing crash injury risk.
Centurion Medical is recalling CVC Bundle VanTex kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
Pfizer is recalling 17,832 bags of LMD in Dextrose Injection due to a potential leak that compromises sterility.
Roche Diagnostics is recalling Tina-quant sTfR assays due to updated claims regarding rheumatoid factor interference.
AZIYO BIOLOGICS is recalling CanGaroo Envelopes because sutures may become brittle or break before expiration. The devices are used to secure cardiac and neurostimulator implants.
Becton Dickinson is recalling BD Microtainer SST tubes because damaged reservoirs may cause insufficient sample volume and erroneous test results.
Diamond Crystal Brands is recalling Chef's Companion Instant Chocolate Mousse Mix because it contains soy lecithin that is not declared on the label.
Centurion Medical Products is recalling Triple Lumen CVC kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate from the sealed surface after disconnection.
Centurion Medical Products is recalling OR VANTEX kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate after disconnection.
Weaver Fundraising is recalling Trail's End Chocolatey Carmel Crunch tins due to undeclared almonds, cashews, and pecans.
Epic Pharma is recalling Estradiol 0.5 mg tablets because 1 mg tablets were found in the bottles. Patients should stop using the product and contact their healthcare provider.
Centurion Medical Products is recalling CVC Insertion Bundles because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
Centurion Medical Products is recalling CVC bundles containing BD MaxZeroNeedleess Connectors due to a risk of fluid droplets separating from the connector surface.
Centurion Medical Products is recalling UVC Trays containing BD MaxZeroNeedleess Connectors due to a risk of fluid droplets separating from the connector surface.
Centurion Medical Products is recalling Invasive Procedure Trays because they include a recalled connector that may release fluid droplets.