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.
Morrilton Packing Co. is recalling approximately 12,146 pounds of boneless ham products because they contain soy, a known allergen, that was not declared on the label.
Brett Anthony Foods is recalling Green Quinoa Cous Cous Salad kits because consumers found a piece of wire in the product.
Baylis Medical Corp is recalling 433 ProTrack Microcatheters nationwide due to circumferential cracks along the shaft.
Save-A-Lot is recalling 16-ounce bags of Whole Kernel Corn Frozen Fresh because a sample tested positive for Listeria monocytogenes.
Carl Zeiss Meditec is recalling IOL Master 500 software versions 7.5 and 7.7 because calculation printouts and exported reports may contain incorrect intraocular lens power data.
Save-A-Lot is recalling Wylwood Mixed Vegetables Steam Bags because a sample tested positive for Listeria monocytogenes. The product was distributed to specific states in the US.
Ameritrans is recalling 2012-2014 buses with Ricon wheelchair lifts where oversized pivot holes may allow bearings to shift, risking platform failure.
Life Science Pharmacy Inc. is recalling compounded Estriol Vaginal Creams due to potential penicillin cross-contamination.
Philips Medical Systems is recalling BuckyDiagnost patient support materials because the footplate hook may fail, causing the plate to fall or swing and injure patients or operators.
Brookshire Brothers is recalling David's Gourmet Chocolate Chunk Pecan Cookies due to plastic found in the cookie dough.
Philips is recalling eight INTEGRIS cardio systems because the ceiling suspension system may fall.
Philips Medical Systems is recalling patient support materials for the EasyDiagnost device because the footplate hook may fail, causing the footplate to fall or swing and potentially injure patients or operators.
Western Drug is recalling Cantharitus Multi-Mix Prep because the product lacks assurance of sterility. The recall affects all lots distributed nationwide.
Western Drug is recalling T.C.A 30% Acid Solution because the product lacks assurance of sterility. The recall affects one container distributed nationwide.
Medtronic is recalling InSync III pacemakers due to unexpected high battery impedance affecting long-term performance.
Philips Medical Systems is recalling 10 Xper vascular systems because the monitor ceiling suspension system may fall.
Carl Zeiss Meditec AG is recalling IOL Master 5.5 software versions 7.5 and 7.7 because printouts and reports may contain incorrect IOL power data.
Philips Medical Systems is recalling INTEGRIS H5000F/Allura 9F X-ray systems because the monitor ceiling suspension system may fall.
Life Science Pharmacy Inc. is recalling compounded Estriol Gels because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Philips Medical Systems is recalling nine Allura Xper Series units because the monitor ceiling suspension system may fall.
Life Science Pharmacy Inc. is recalling Human Chorionic Gonadotropin (HCG) sublingual drops due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.
Philips Medical Systems is recalling five Allura BiPlane X-ray systems because the monitor ceiling suspension system may fall.
Shakti Group USA LLC is recalling 39,450 lbs of ground cumin because it contains 8.0 ppm of peanut allergen. The product was distributed in New York.
Quest Medical, Inc. is recalling specific MPS Delivery Sets used with cardiopulmonary bypass equipment due to intermittent seal failures during use.
DeRoyal Industries is recalling 836 sterile custom surgical kits because a component may have packaging seal defects that compromise sterility.