State
72,940 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.
Which agencies issued them
These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Volkswagen is recalling 3,138 model year 2025 Tiguan vehicles because a fault in the passenger occupant detection system wiring may deactivate the front passenger air bag when the seat is occupied.
Philips North America is recalling the IntelliVue MP50 over a potential issue where the monitors did not alarm.
Pacific Seafood is recalling 15,498 lbs of Raw Blackened Shrimp because the shrimp may contain 3.4mg sulfur dioxide per serving and the label does not declare sulfite.
Philips North America is recalling the IntelliVue Patient Monitor MX850 over a potential issue where the monitors did not alarm.
Breckenridge Pharmaceutical is recalling 7,389 bottles of Duloxetine Delayed-Release Capsules, 60 mg, over the presence of N-nitroso-duloxetine above the FDA recommended limit.
Great Lakes Cheese is recalling 4,131 cases of mozzarella and provolone shredded cheese blend, sold under four brands, over potential metal fragments from a supplier raw material.
Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Multi Measurement Server X2 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Great Lakes Cheese is recalling 117 cases of Food Club Finely Shredded Pizza Style Four Cheese Blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
Costco is recalling 612 retail units of Kirkland Signature Chicken Sandwich with Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Great Lakes Cheese is recalling 235,789 cases of low-moisture part-skim mozzarella shredded cheese, sold under 26 brands, over potential metal fragments from a supplier raw material.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement because the product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.
Illumina is recalling 11,916 NextSeq 550Dx reagent kits because flow cell gaskets have a quality issue that may cause leaks during runs, including possible toxic substance exposure to the user.
Costco is recalling 142,532 retail units of Kirkland Signature Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Great Lakes Cheese is recalling 1,850 cases of Good & Gather Mozzarella & Parmesan shredded cheese blend over potential metal fragments originating in a supplier raw material.
Philips North America is recalling the IntelliVue MP2 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX400 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP70 over a potential issue where the monitors did not alarm.
Avion Pharmaceuticals is recalling 804 bottles of Prenate Chewable after positive test results for soy, which is not listed on the label, and a boron amount stated in mg instead of mcg.