Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
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.
Ferrari is recalling specific 458 and 488 models because the brake system may leak fluid, potentially causing a loss of braking ability.
Forest River is recalling certain 2021-2022 XLR Toy Hauler recreational vehicles with a missing protective panel between the furnace and cargo area. The missing panel could allow cargo to contact furnace wiring, creating a fire hazard.
AFFCO USA is recalling approximately 24,461 pounds of frozen raw lamb shoulder products that were imported without the required re-inspection.
Orange EV is recalling 2019-2021 T-Series electric trucks because a steering bolt may loosen, potentially causing loss of steering.
Red Medical Supplies is recalling EcoGel 100 ultrasound gel due to possible bacterial contamination. Approximately 639 units were sold nationwide through Amazon.com.
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. Products distributed nationwide in the U.S., Canada, and other locations have been recalled.
Abbott Molecular has recalled 71,314 units of the Alinity m SARS-CoV-2 Amp Kit due to potential false positive results. The kit was distributed worldwide.
SSM Health Care St. Louis is recalling 385 bags of Potassium Chloride 40 mEq in 0.9% Sodium Chloride injection due to lack of assurance of sterility. The affected lot was distributed in Missouri.
Eco-Med Pharmaceutical's ultrasound gel products are recalled due to potential bacterial contamination. The FDA advises healthcare providers to stop using the affected product.
Abbott Molecular recalls its Alinity m SARS-CoV-2 Amp Kit (Non-US Assay), an in vitro diagnostic test, due to potential for false positive results. Approximately 11,408 units were distributed worldwide.
Abbott Molecular is recalling 60,563 units of the Alinity m SARS-CoV-2 Amp Kit due to potential false positive test results. The affected kits were distributed worldwide from September 2021 through January 2023.
Doosan Portable Power is recalling 2019-2021 Mobile Generators and Air Compressors because improperly tightened wheel lug nuts could cause a tire to fall off, increasing crash risk.
Eli Lilly is recalling Glucagon Emergency Kits (Lot #D239382D, expiration April 2022) because some vials contain liquid instead of powder and do not deliver the full expected drug effect when administered.
FDA recalls ultrasound gels manufactured by Eco-Med Pharmaceutical due to possible bacterial contamination. Healthcare providers and facilities should stop use immediately.
Ultrasound gels and lotions from National Distribution & Contracting Inc are being recalled due to potential bacterial contamination. About 25,103 units distributed nationwide and in Canada are affected.
Abbott is recalling the Alinity m Resp-4-Plex AMP Kit, an in vitro diagnostic used for respiratory pathogen testing, due to potential for false positive results affecting approximately 8,469 units distributed worldwide.
Cuisine Innovations Unlimited, LLC is recalling Vemondo Vegan Crabless Mini Crabcakes sold at Lidl due to undeclared egg. The product may pose a risk to consumers with egg allergies.
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit due to potential false positive results. The recall affects 5,855 units distributed worldwide.
Newmar is recalling 2020-2022 Essex, King Aire, and London Aire motorhomes due to a power steering pump machining defect that can result in loss of steering assist and increased crash risk. Affected owners should contact Newmar for free inspection and replacement.
Braun recalls 2020-2021 Chevrolet Traverse wheelchair vehicles for a transmission fluid leak hazard. A faulty screw and clip may cause fluid loss, risking power loss, crashes, and fire.
Triple E is recalling specific 2015-2018 recreational vehicles because the refrigerator exhaust vents directly onto the wood frame, which can overheat and ignite.
Schwarze is recalling 2012-2020 M6 Avalanche street sweepers because an outside switch box may activate unintentionally, creating a crushing hazard.
Volkswagen is recalling certain 2021 Atlas, Atlas Cross Sport, and Passat vehicles because the front wheel bearing bolts may have been incorrectly tightened and could loosen, potentially causing loss of control and crash risk.
Yamaha is recalling 2020-2021 XVS950 motorcycles because the engine case may leak oil onto the rear tire, increasing the risk of a crash.
Trail King is recalling 2015-2020 AACS and ACS trailers because rear suspension beams may crack and detach, increasing crash risk.