State
73,584 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, 1,131 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,602 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,372 recalls whose distribution notice names Alabama specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Teligent Pharma is recalling Econazole Nitrate Cream 1% in 85-gram bulk tubes due to incorrect labeling. The product was distributed nationwide.
Spirit Pharmaceuticals is recalling Acetaminophen 325 mg Regular Strength Pain Reliever tablets due to discoloration and current good manufacturing practice (cGMP) deviations. The recall affects one lot distributed nationwide.
Dr. Reddy's Laboratories is recalling Tizanidine HCl 4 mg tablets nationwide because some tablets are shaved, failing the required tablet specification.
Teligent Pharma is recalling Triamcinolone Acetonide Ointment USP 0.1% due to a labeling mispack affecting Lot #16630 with expiration 03/2023. The recall was issued due to incorrect labeling on the product.
Wee Gallery is recalling Ocean and Safari animal wooden tray puzzles because the octopus and elephant puzzle pieces can break, posing a choking hazard to young children.
PL Custom is recalling 2019 Dodge RAM 5500 emergency vehicles because rear brake lines may wear, risking brake loss and crashes.
Crane Carrier is recalling 94 LET2 vehicles from 2020-2021 because a fuel hose may leak, increasing the risk of fire if exposed to an ignition source.
Dorel is recalling Maxi-Cosi Pria 85 convertible child seats because they may not adequately protect children from head injury if installed with only a lap belt.
Reitnouer is recalling 2017-2019 Steer Axle trailers because the steering arm may detach, potentially causing loss of control or road hazards.
Ford is recalling 2021 F-150 Super Cab vehicles because front seatbelt webbing may be incorrectly routed, increasing injury risk in a crash.
PL Custom is recalling one 2021 Ford E-450 emergency vehicle because its LCD display may freeze or fail, potentially delaying emergency efforts.
Ford and Lincoln are recalling certain 2021 Explorer and Aviator vehicles. Side air bag attachment weld studs may detach during deployment, potentially failing to provide proper protection in a crash.
General Motors is recalling certain 2016-2021 Chevrolet Malibu and 2019-2021 Cadillac XT4 vehicles because rear seat belt retractors may be improperly secured with loose or missing fasteners, potentially affecting safety in a crash.
General Motors is recalling 2020-2022 Chevrolet Bolt EV and 2022 Bolt EUV vehicles. The high-voltage battery could catch fire when charged to full or nearly full capacity, increasing risk of injury.
Volkswagen is recalling certain 2022 Taos vehicles because the underhood fuel supply quick-connector may detach from the fuel line, creating fuel leaks that increase risks of engine stalling and fire.
PACCAR is recalling certain 2021-2022 Peterbilt commercial trucks due to insufficient clearance in the Hill Start Assist valve assembly, which may damage the rear brake hose and disable rear braking. Dealers will inspect and repair the assembly free of charge.
Deere & Company is recalling approximately 200 John Deere compact utility tractors (models 4044M, 4044R, 4052M, 4052R, 4066M, 4066R) because rear wheel spacer bolts can be improperly torqued during manufacturing, causing the wheel to fall off and the tractor to overturn.
Space Craft is recalling Lippert 6400 series vented windows because the adhesive may fail, causing the vent to detach and increasing crash risk.
Frieyss infant bath seats fail to meet federal safety standards and can tip over while in use, posing a drowning hazard to babies. About 120 units were sold exclusively online at Amazon.com from March through April 2021.
Medtronic is recalling the HeartWare HVAD Driveline Extension Cable (443 units) due to higher frequency of neurological adverse events and mortality in clinical comparisons with other heart assist devices. The pump may experience restart delays or failures.
Heartware is recalling HVAD Pump Accessories due to clinical data showing higher rates of neurological adverse events and mortality compared to other left ventricular assist devices, and reports of pump malfunctions.
Medtronic is stopping the HVAD System due to observational data showing higher mortality rates and neurological adverse events compared to other cardiac assist devices. The internal pump may also delay or fail to restart.
Medtronic is recalling the HeartWare HVAD heart pump implant due to higher rates of neurological adverse events and mortality compared to other devices. The internal pump may also delay or fail to restart.
Medtronic is recalling the HeartWare HVAD Pump Implant Kit due to higher rates of neurological adverse events and mortality compared to other heart pump devices. The pump may also delay or fail to restart.
Medtronic recalled the HeartWare HVAD Implant Kit due to higher rates of neurological adverse events and mortality compared to other left ventricular assist devices. The pump may also fail to restart.