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.
Thor Motor Coach is recalling 2020 Sequence 20L motorhomes because solar panel screws may fail, causing the panel to detach and create a road hazard.
New York Style Sausage Co. issued a public health alert for raw pork bangers containing undeclared sesame seed. No illnesses have been reported.
Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because missing seat recliner parts may reduce occupant restraint in a crash.
Mercedes-Benz is recalling 24,226 vehicles due to a software fault that may cause the emergency call system to relay inaccurate location data, potentially delaying emergency responders.
Mercedes-Benz is recalling 29,720 vehicles because front seat belts may be incorrectly detected as unfastened, potentially disabling safety features.
John Deere is recalling 4044R, 4052R, and 4066R compact utility tractors because improperly torqued front cab support bolts can fail during a rollover, posing a crushing injury hazard.
New Port Sales is recalling All-Gloo Craft Glue because the packaging does not meet child-resistant closure requirements, posing a poisoning hazard to children.
GN Otometrics is recalling 3,071 ICS CHARTR EP 200 units because undergrounded electrical surfaces may cause electrical shock to patients or healthcare professionals.
Infinite Herbs, LLC is recalling conventional basil potentially contaminated with Cyclospora. The product was distributed to one retail customer and three distributors.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may separate during use in specific legacy devices.
Andover Healthcare Inc. is recalling 1,759 cases of sterile Co-Flex LF2 wound dressings because of incomplete packaging seals, which may compromise sterility.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may become loose and separate from the canister body during use.
Kawasaki is recalling about 1,100 lawn mower engines because a damaged fuel line can leak fuel, posing burn and fire risks.
Community Products is recalling 1,079 Rifton TRAM Low Base powered lift devices because a design change makes the latch springs susceptible to fatigue failure.
GE Healthcare is recalling ApexPro Telemetry Server Systems because they may fail to provide visual or audible alarms for ECG arrhythmias, lead failures, or pulse oximetry issues.
Smiths Medical ASD Inc. is recalling GRIPPER Needles because some may be occluded or blocked, posing a risk to patients.
Abbott Laboratories is recalling 22 CELL-DYN Emerald analyzers with diluent tubing that appears cloudy or has a film, which may cause falsely elevated platelet results.
Temp-Air is recalling 2017-2019 EBB-80 trailers because an incorrect hitch coupling may limit adjustability, potentially causing the trailer to drag and increasing crash risk.
Beckman Coulter is recalling Lipase assays because acetaminophen metabolites cause negative interference in overdose patients.
OMNIlife science Inc. is recalling three OMNI Hip System femoral components because they are missing the required porous coating.
Brainlab is recalling Patient Data Manager software versions 2.1.1 through 2.5.1 because segmentation shifts may not be reflected in DICOM exports.
Community Products, LLC is recalling 3,282 Rifton TRAM Standard Base powered lift devices due to a design defect that may cause the latch mechanism to fail after repeated use.
Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.
Becton Dickinson is recalling 1.7 million BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the needle retracts.
Beckman Coulter is recalling Uric Acid assays because acetaminophen metabolites cause negative interference in overdose patients.