State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Gillig is recalling 2,732 Low Floor transit buses because wiper arms can crack and detach, reducing driver visibility and increasing crash risk.
Pier 1 Imports is recalling Neely and Dahlia bistro chairs because loose bolts can cause the legs to collapse, posing a fall hazard.
Manac is recalling 2016-2017 Van Trailers because aluminum rivets securing external rub rails may fail, allowing the rails to detach and become road hazards.
RDG Global is recalling about 2,600 girls' hooded sweatshirts sold at Nordstrom because the hood drawstrings pose a strangulation hazard to children.
Shearers Foods is recalling Larry The Cable Guy Biscuits & Gravy Thin Potato Chips because ingredients may be contaminated with Salmonella.
Pacific Medical Solutions is recalling Nano PNC Water because it was marketed without FDA approval and tested positive for the bacterium variovorax paradoxus.
Shearers Foods is recalling Deep River Sour Cream & Onion Krinkle Kettle Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
Shearers Foods is recalling specific bags of nacho cheese tortilla chips because they contain ingredients from a supplier that may be contaminated with Salmonella.
Shearers Foods is recalling Delish Jalapeno White Cheddar Potato Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
Shearers Foods is recalling Spicy Nacho Cheese Tortilla Chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.
Shearers Foods is recalling its Larry The Cable Guy jalapeño popper chips because ingredients from Valley Milk Product may be contaminated with Salmonella.
Olympus is recalling URF-P6 and URF-P6R uretero-reno fiberscopes due to adverse events involving tissue trauma and stuck insertion tubes reported in similar devices.
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles because front seat belt linkages may detach from anchor pretensioners, increasing injury risk in crashes.
United Exchange Corporation is recalling 190,710 bottles of Eye Wash due to a lack of assurance of sterility. The product was distributed nationwide, in Puerto Rico, and in Guyana.
Medtronic is recalling 22,298 SynchroMed II software application cards to update the priming bolus function and pump labeling.
United Exchange Corporation is recalling 112,320 bottles of Eye Irrigating Solution because the product lacks assurance of sterility.
United Exchange Corporation is recalling 77,184 bottles of Eye Wash because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide, in Puerto Rico, and in Guyana.
Volkswagen is recalling 2007-2010 Touareg vehicles because a fuel filter flange may crack and leak fuel, increasing the risk of fire.
Mylan Pharmaceuticals is recalling 1,338 bottles of Glipizide 5 mg Extended-Release Tablets because they may contain 10 mg tablets.
Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.
Beckman Coulter is recalling iChemVELOCITY Urine Chemistry Systems because probe misalignment or bending can lead to delayed or incorrect patient results.
Cook Inc. is recalling 854 Check-Flo Performer Introducer Sets because a specific valve design is associated with increased reports of blood loss.
Siemens is recalling specific Calibrator A Kits due to a negative bias in FT4 assays and potential calibration failures on certain systems.
Cook Inc. is recalling 29 Check-Flo Introducer Hausdorf-Lock Atrial devices worldwide due to increased reports of blood loss associated with the hemostatic valve design.