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.
C. O. Truxton is recalling Phenobarbital 15 mg tablets that were actually 30 mg due to a labeling error.
C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 30 mg, because they may be mislabeled. The FDA classifies this as a Class I recall.
Commonwealth Dairy is recalling Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt because it may contain undeclared almond pieces.
Bush Brothers & Co is recalling 28-ounce cans of Country Style Thick, Rich Sauce with Bacon & Extra Brown Sugar due to defective side seams that may allow C. botulinum growth.
Solta Medical is recalling four VASER Amplifier units because a service depot repair may have caused inaccurate calibration, posing a burn risk to patients.
Erwin Hymer is recalling 2016-2018 Hymer Aktiv recreational vehicles because the exhaust pipe may melt the rear bumper and wiring, increasing crash and burn risks.
The Harvard Drug Group is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.
Bush Brothers & Co is recalling Bush's Best Baked Beans due to defective side seams that may allow C. botulinum growth.
The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.
Bush Brothers & Co is recalling Bush's Best Brown Sugar Hickory Baked Beans due to defective side seams that may allow C. botulinum growth.
The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.
The Harvard Drug Group is recalling Rugby Senexon Liquid due to microbial contamination, including yeast and potential B. cepacia.
Medtronic is recalling 60 reusable ENT suction instruments because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Custom Assemblies Inc is recalling 2,155 custom surgical kits because they contain BD SafetyGlide needles with loose polypropylene particulate in the fluid path.
Penobscot McCrum LLC is recalling Sysco X-Large Jo-Jo Wedges because the product may contain undeclared milk.
Penobscot McCrum LLC is recalling Extra Large Coated Jo-Jo Wedges because the product may contain undeclared milk.
REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.
Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.
Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.
Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.
Penobscot McCrum LLC is recalling Extra Large Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.
Solta Medical is recalling seven VASER PRO Amplifiers because a service depot repair may have caused inaccurate calibration, posing a risk of patient burns.