State
73,598 recalls have nationwide distribution and so reach Alabama. 6,372 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,372 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,604 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,372 recalls whose distribution notice names Alabama specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Teva Pharmaceuticals is recalling 1,416 vials of Romidepsin Injection because stability testing revealed out-of-specification impurities.
Curt Manufacturing is recalling specific Forged Ball and Pintle Hitches because a defect may cause the towed vehicle to separate, increasing crash risk.
Volkswagen Group of America is recalling specific Audi A3 and S3 models because the passenger air bag may deactivate while the seat is occupied.
Avanza Pasta, LLC is recalling approximately 9,847 pounds of beef and poultry ravioli and tortellini produced without federal inspection. No adverse reactions have been reported.
Airstream is recalling 2017-2020 Basecamp travel trailers because air conditioner mounting bolts may loosen or break, allowing the unit to separate from the roof.
Isuzu is recalling 2015-2021 Isuzu, Chevrolet, and International trucks because rear axle U-bolt nuts may loosen, causing axle misalignment and potential loss of power.
Mercedes-Benz is recalling specific 2014-2020 models equipped with panoramic sunroofs because the front roof panel may not have been bonded correctly during a prior repair.
Mercedes-Benz is recalling 11,356 vehicles because the sunroof glass may detach, creating a road hazard and increasing crash risk.
USDA FSIS issued a public health alert for specific beef and lamb products from One Meat Corp. that were produced without federal inspection.
ARBOC is recalling 2018-2021 Spirit of Equess buses because incorrect engine software may fail to limit speed or torque, increasing crash risk.
General Motors is recalling 2021 Chevrolet Express and GMC Savana vans with 6.6L engines because a battery cable defect may cause a short circuit and fire.
Arcimoto is recalling 2019-2020 FUV and 2020 Deliverator vehicles because high-voltage contactors may overheat, causing unexpected battery shutdowns and loss of motive power.
HD Hudson is recalling illu-Mist battery-powered garden sprayers because the lithium-ion battery can overheat and catch fire. Consumers should stop using the sprayers and contact the company for a replacement.
General Motors is recalling 2021 full-size SUVs because third-row seat belts may be entrapped or misrouted behind the seat-folding mechanism, potentially becoming damaged. A damaged seat belt could break during a crash, increasing the risk of occupant injury.
Briggs & Stratton is recalling YTL log splitters with 250cc engines due to a risk of engine kickback causing injury. Two incidents involving broken wrists have been reported.
Parker Squared is recalling Shepherd Boy plush toys because the wire in the shepherd's staff can become exposed, posing a laceration hazard.
Tiffin is recalling certain 2021 Phaeton recreational vehicles because the valve stem stabilizer can become loose, allowing the valve stem extender to contact the wheel, which can cause tire pressure loss and increase crash risk.
General Motors is recalling certain 2021 Chevrolet Camaro vehicles because the left or right axle shaft may be missing a retaining ring, which could separate during driving and cause loss of power, increasing crash risk.
Genentech is recalling Evrysdi prescription bottles that may leak due to a fit issue, posing a risk of drug exposure through skin or eye contact.
RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.
Draeger Medical is recalling VentStar Anesthesia breathing circuits because the Y-piece may detach, causing a leak that hinders patient ventilation.
Medtronic Vascular is recalling 10 units of 6F Launcher Guide Catheters because unsealed pouches may compromise sterility.
RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.
RTI Surgical is recalling specific batches of the CervAlign Anterior Cervical Plate System because the locking mechanism may disassociate, requiring revision surgery.
Medtronic Vascular is recalling 9 units of 6F Launcher Guide Catheters because unsealed pouches may compromise sterility.