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.
Zimmer, Inc. is recalling 19 Continuum Acetabular System hip prosthesis shells because they are missing polar boss threads.
Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.
Plum, Inc. is recalling Little Cremes organic rice milk snacks because they are not softening as intended, posing a choking hazard to babies and young children.
Hospira Inc. is recalling 145,600 vials of Hydromorphone Hydrochloride Injection because customer complaints confirmed that some glass vials may be broken or cracked, compromising sterility.
Ad-Tech Medical Instrument Corporation is recalling Cueva Electrode Kits because the applicator wand may malfunction, potentially preventing monitoring of the VII cranial nerve.
Meritor Wabco is recalling specific Quick Release Valves where damaged rubber diaphragms may reduce air pressure, potentially compromising braking performance.
Hino is recalling 2,641 model year 2012-2015 XJC and XFC trucks because a software issue may prevent the brake warning lamp from illuminating, increasing crash risk.
Halcore is recalling 2006 Leader Type II Ambulances equipped with specific Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
Meijer is recalling Halloween projector flashlights because they can overheat and melt the plastic handle, posing a burn risk to users.
Morgan Olson is recalling 100 model year 2014 Mercedes-Benz Sprinter 2500 vehicles because an aluminum document holder may injure unbelted occupants in a crash.
Mazda is recalling 2014-2015 Mazda6 vehicles because the tire pressure monitoring system may fail to warn drivers if all four tires lose pressure simultaneously, increasing crash risk.
Volkswagen is recalling 2015 Jetta and Passat vehicles because a seatback recliner bracket may not engage correctly, causing unexpected movement that could distract the driver.
Daimler Trucks North America is recalling 2015 Thomas Built Buses Saf-T-Liner HDX school buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Taylor Farms is recalling approximately 377 pounds of Signature Café Broccoli Kale Salad with Chicken because the product contains undeclared walnuts, a tree nut allergen.
Bumble Bee Foods is recalling Sun Dried Tomato pouches because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna due to seal defects that could allow contamination by spoilage organisms or pathogens.
Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer because they are damaged and can cause electric shock.
Merge Healthcare is recalling eFilm Workstation versions 4.0 and 4.0.1 because a software defect may cause users to select the wrong patient study when using the thumbnail panel.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Bumble Bee Foods is recalling specific codes of pouched Albacore tuna because seal defects could allow contamination by spoilage organisms or pathogens.
Biomet is recalling six Discovery Elbow Humeral Trials that were incorrectly manufactured as left-sided but etched as right-sided.
Gulf States Toyota is recalling 142 model year 2015 Toyota Tacoma vehicles because they may have incorrect load carrying capacity labels, which could lead to vehicle overload.
Invivo Corporation is recalling 24 Philips Expression MR200 MRI Patient Monitoring Systems because they may fail to produce Non-Invasive Blood Pressure (NIBP) measurements.
Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer due to damage that can cause electric shock.