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.
BMW is recalling 2015 MINI Cooper Hardtop 2 Door vehicles because the seatback adjustment mechanism may not be fully engaged, increasing injury risk in a rear impact.
Kulana Foods is recalling approximately 4,465 pounds of frozen, fully cooked pork products because they contain wheat, a known allergen, that is not declared on the label.
Dynamic Tire Corp. is recalling specific Towmax STR tires with incorrect load and pressure markings that could lead to overinflation and tire failure.
Ford is recalling 2014 F-150 and Flex vehicles because a seat defect may cause the passenger airbag to fail to deploy in a crash.
Jaguar is recalling 2014-2015 F-TYPE vehicles because a wiring error may prevent the front passenger airbag from deactivating when a child or small adult is present.
Chrysler is recalling 2014-2015 Dodge Journey vehicles because tire placard labels may contain inaccurate weight and seating information, increasing crash risk.
Hyundai is recalling 2009-2011 Genesis and 2011 Equus vehicles because a circuit failure may prevent stop lamps from illuminating, increasing the risk of a rear-end crash.
4Seasons is recalling folding lounge chairs sold at Ross Stores because they can tip or recline too quickly, posing a fall hazard.
Martin Avenue Pharmacy is voluntarily recalling Acetylcysteine 10% inhalant solution due to quality control observations that present a risk to sterility assurance.
Cummings Mobility is recalling wheelchair lifts on certain 2006-2014 vans because platform side plates may crack, posing an injury risk.
Joerns Healthcare is recalling 3,135 EasyCare Beds because the Care-Lock feature may fail to stay engaged, posing a safety risk to patients.
Martin Avenue Pharmacy is voluntarily recalling Bupivacaine hydrochloride 0.25% injectable vials due to quality control observations that present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Tri-mix T102 injectable vials because quality control issues identified during an FDA inspection may compromise sterility.
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations due to quality control observations that present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Tri-mix injectable vials because quality control observations during an FDA inspection raised concerns about sterility assurance.
Good Herbs, Inc. is recalling Bee Formula bottles because they were not manufactured under Good Manufacturing Practices (GMPs).
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including morphine/bupivacaine, due to quality control issues affecting sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Glycerin 72% sodium chloride injectable vials due to quality control observations that risk sterility assurance.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator C kits due to a realignment issue with Ferritin Analytical Sensitivity. The recall affects 234 kits distributed worldwide.
Merge Healthcare is recalling 52 Hemo Programmable diagnostic computers because the SpO2 and heart rate values displayed may not update to reflect changes in the patient's condition.
Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including triamcinolone acetonide, due to quality control observations that risk sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling all compounded sterile preparations within expiry due to quality control observations that present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Lidocaine 2% injectable vials because quality control observations during an FDA inspection raised concerns about sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling PGE 4 injectable vials because quality control issues identified during an FDA inspection present a risk to sterility assurance.
Martin Avenue Pharmacy is voluntarily recalling Tri-mix injectable vials due to quality control observations that present a risk to sterility assurance.