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.
The Anspach Effort, Inc. is recalling 99 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual usage, potentially resulting in greater exposure than specified.
The Anspach Effort, Inc. is recalling 138 fluted drum dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
Winnebago is recalling 2012-2016 Era recreational vehicles because certification labels list incorrect front tire inflation pressures, which could lead to tire failure.
The Anspach Effort, Inc. is recalling 177 fluted drum dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 72 Anspach Extra Coarse Diamond Ball tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure.
Dairy Farmers of America is recalling specific Sandwich Mate cheese slices because a piece of plastic film might remain attached to the product.
Oxysure Systems is recalling 1,005 Model 615 oxygen cartridges because they do not meet FDA flow rate standards.
Ameritrans is recalling 2015 225 vehicles because the back-up camera may display reversed images, increasing the risk of a crash.
John Deere is recalling specific riding lawn tractors because a brake arm can fail, posing a crash hazard that could result in serious injury or death.
Forest River is recalling 2015-2016 Cedar Creek Silver Back recreational vehicles because the gross vehicle weight rating on the certification label is incorrect.
Manhattan Group is recalling My Snuggly Ellie Activity Toys because the wooden ring can break into small pieces, posing a choking hazard to young children.
USDA FSIS issued a public health alert for whole pigs used for roasts due to possible Salmonella contamination linked to illness clusters in Washington.
Stork Craft is recalling about 18,500 foam crib mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Nipponflex is recalling about 400 Smart Flex and Smart Care mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Forest River is recalling 160 motorhomes because the back-up camera system may display reversed images, increasing the risk of a crash.
Liftmoore is recalling 2001-2006 6036WX truck cranes because a specific battery equalizer part may conduct electricity when heated, increasing fire risk.
Forest River is recalling 2014-2016 Sandpiper and Sierra recreational vehicles because inaccurate gross vehicle weight rating labels could mislead owners about capacity.
ACCO Brands is recalling about 3.3 million Quartet magnetic and dry erase boards because sharp metal edges on the back can cause lacerations when removing the boards.
Heartland is recalling various trailer models because tire certification labels may contain inaccurate sizing or inflation information, potentially leading to tire failure.
The FDA is recalling 77,588 sterile single basin kits because the Devon Light Gloves contain splits or holes that compromise sterility.
FDA is recalling sterile Major Kits containing Devon Light Gloves due to splits or holes that compromise sterility.
Biomet Spine is recalling 4,765 units of Polaris 4.75 TI Spinal System multiaxial screws because they may not meet internal fatigue strength requirements.
DePuy Orthopaedics is recalling ATTUNE Knee Tibial Articulation Surface Instruments because a small wire spring coil (Balseal) may detach and be left in the patient during surgery.
Bausch & Lomb is recalling SoFlex SE foldable intraocular lenses because haptics may break during loading and insertion.
Honda is recalling 2013-2015 CB500 and CBR500 motorcycles because a fuel sensor defect may cause the vehicle to stall, increasing crash risk.