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.
Bard Peripheral Vascular Inc is recalling 13 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Elekta is recalling 49 Monaco Radiation Treatment Planning Systems because software errors display and export incorrect anatomy and beam shift directions.
The Beaufort Bonnet Company is recalling handmade knit dolls because a sewing needle was found in the stuffing, posing a puncture injury risk.
RH is recalling about 3,200 children's chairs and stools sold in the U.S. and Canada because the paint contains lead levels exceeding federal bans.
NHTSA is recalling 2020 Coachmen Catalina travel trailers because short fasteners may allow upper sleeping bunks to fall, posing an injury risk.
RH is recalling about 5,400 Ultra-Soft Turkish robes because they fail federal flammability standards, posing a burn risk. Consumers should stop using them and request a refund.
Heatherfield Foods is recalling pork sausage products labeled as gluten-free that contain wheat. The recall affects retail locations in Hawaii.
WAYB is recalling Pico child seats manufactured between February and August 2019 because the headrest frame can break and detach, increasing injury risk in a crash.
GreatCall is recalling Lively Mobile Plus emergency alert devices because the call button may fail during an emergency. No injuries have been reported.
Indian Motorcycle is recalling 2019 Chieftain models because tail lights may be too bright, potentially confusing other drivers and increasing crash risk.
Decathlon USA is recalling about 50 Rocky Screwgate carabiners because incorrect assembly can cause them to unlock while in use, posing a risk of serious injury or death.
Pearhead is recalling Ubbi Connecting Bath Toys because they can break and create sharp points, posing choking and laceration hazards to young children.
FCA US is recalling 2019 Ram 2500 and 3500 trucks because incorrect assembly fluid in brake calipers may cause seals to swell, leading to dragging brakes and increased crash risk.
Sandoz is recalling approximately 636,000 bottles of Losartan Potassium and Ezetimibe because the caps do not meet child-resistant requirements, posing a poisoning risk to children.
Rite Aid is recalling about 18,800 folding patio chairs because the frames can bend, causing users to fall and potentially get injured.
Green Water, LLC is recalling specific lots of Taspen's Organics herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
SIGA Logistics is recalling 1 lb bags of fresh basil due to potential Cyclospora contamination. The product was distributed in several US states.
Siemens Healthcare Diagnostics is recalling N Cuvette Segments for the BN ProSpec System because they may produce falsely elevated albumin results.
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Green Water, LLC is recalling Taspens Organics tea and herbal tinctures due to potential Salmonella contamination. The products were distributed nationwide.
Thoratec Corp. is recalling 149 Heartmate 3 Sealed Outflow Graft units because the C-Ring may not seat properly, causing leaks during implantation.
TiSport is recalling 1,452 TiLite wheelchairs because the anti-tip tubes may fail, allowing the chair to tip backwards.
Elevation Foods is recalling Fresket egg salad because Listeria monocytogenes was found in the product. The recall covers specific cases distributed to multiple states.
Siemens is recalling IMMULITE 2000 Progesterone tests because some samples may produce falsely low results, potentially leading to unnecessary medication.