State
73,809 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,378 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 1,605 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Beanworthy is recalling Human Creations EnergyFlux battery chargers and hand warmers sold on Amazon due to a fire and burn hazard.
Mercedes-Benz is recalling certain 2016-2018 GLC models because rear seat belt latch plates may retract into the interior paneling, preventing use.
Southwire is recalling WiOn Indoor In-wall Wi-Fi Switches because they can overheat and pose a fire hazard. No injuries have been reported.
Louis Garneau is recalling specific Course bicycle helmets because they do not meet federal impact safety standards, posing a risk of head injury.
Pagani is recalling 2017 Huayra Coupe BC and Roadster vehicles because battery management software may prevent the car from starting or idling, increasing crash risk.
Handi-Craft is recalling Dr. Brown's Lovey pacifier and teether holders because the snap can detach, posing a choking hazard to young children.
eheat is recalling about 35,000 Envi wall heaters sold in the U.S. and Canada due to a defect that can cause overheating, smoke, or melting, posing a burn hazard.
Toyota is recalling 2018 Prius C vehicles sold in Puerto Rico because the front passenger air bag and child seating labels may be missing, increasing crash injury risk.
Lotte International America Corp. is recalling Lotte Kancho Choco-Biscuit products because peanut allergen was found during product sampling and testing.
Ferrara is recalling 2004-2012 Inferno and Igniter emergency vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.
Kovatch Mobile Equipment is recalling specific KME Predator fire apparatus vehicles because inconsistent machining may cause front axle spindles to crack and fail, potentially leading to wheel separation.
Maserati is recalling 2017 Quattroporte and Ghibli vehicles because an engine software issue may cause the transmission to shift into neutral or the engine to shut off unexpectedly.
Roche Diagnostics is adding a warning to cobas 6000 and 8000 Modular Series Operator Manuals to prevent operator injury during maintenance.
Abbott is recalling ARCHITECT c8000 Cuvette Segments because a detached post can cause falsely depressed patient results on c4000, c8000, and c16000 instruments.
Synthes (USA) Products LLC is recalling 1,144 sterile 2.5 mm Reaming Rods due to potential gaps in the package seal that may compromise sterility.
Abbott Laboratories is recalling cuvette segments for the ARCHITECT Clinical Chemistry system because detached segment posts may cause falsely depressed patient test results.
Medtronic is recalling 449 O-arm O2 Imaging Systems because servicing internal components may cause an electrical short, posing a shock hazard to field service technicians.
Mindray is recalling 2,875 A-Series anesthesia delivery systems due to a software issue that may apply incorrect settings or skip startup leak tests.
Synthes (USA) Products LLC is recalling sterile Light Clips for the Oracle Retractor because potential gaps in the package seal may compromise sterility. The product is used during orthopedic surgery.
Mindray is recalling A7 Anesthesia Delivery Systems because a software issue may cause incorrect settings to be applied or the startup leak test to be skipped.
Zimmer Biomet is recalling 127 Sirus Drill instruments because they may not be adequately cleaned, potentially leading to infection.
Get The Tea is recalling Life Change Fat Burner because the product contains soy, which is not listed on the label.
Philips Medical Systems is recalling 11 Brilliance Big Bore Oncology CT scanners due to software errors that may affect image generation and display settings.
Bausch & Lomb Inc is voluntarily recalling LASEREDGE Knives for ophthalmic surgery because an atypical volume of complaints indicates dull blades. The recall affects products lacking specific electro-polish and penetration force testing.
Philips is recalling 119 Brilliance Big Bore CT scanners due to software errors that may prevent image generation or display incorrect settings.