State
73,737 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,377 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 1,604 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling 139 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Boston Scientific is recalling 66 units of Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Boston Scientific is recalling 271 Advanix Pancreatic Stents because they were labeled with a 36-month shelf life instead of the approved 18-month shelf life.
Abbott is recalling Alinity i accessory kits because environmental stress may cause cracks in the bulk solution level sensor.
Boston Scientific is recalling Advanix Pancreatic Stents labeled with a 36-month shelf life instead of the approved 18-month duration.
Boston Scientific is recalling Guidezilla II Guide Extension Catheters because they may lack a hydrophilic coating, potentially affecting device performance.
Bard Peripheral Vascular Inc is recalling 900 units of PowerPort isp M.R.I. Implantable Ports because they were packaged with the incorrect introducer sheath size.
Avantor Performance Materials Inc is recalling bulk Potassium Phosphate, Monobasic, Crystal due to failed stability specifications for iron content.
AuroMedics Pharma LLC is recalling Amiodarone Hydrochloride Injection vials due to the presence of visible particulate matter (crystallization). The affected lots were distributed nationwide in the US.
Merical, LLC is recalling Leader Advanced Probiotic capsules because the label lists the wrong probiotic blend. Consumers should stop using the product.
AuroMedics Pharma LLC is recalling 28,810 vials of Amiodarone Hydrochloride Injection due to the presence of visible particulate matter.
AuroMedics Pharma LLC is recalling Amiodarone Hydrochloride Injection vials due to the presence of visible particulate matter (crystallization). The affected lots were distributed nationwide in the US.
Piaggio is recalling 399 2020 Moto Guzzi V85 TT motorcycles because footrest mounting clips may break, causing the footrest to fall off and create a road hazard.
Zamzow is recalling one Aero Easy Cover tarping pawl assembly because a missing weld may cause the part to separate, increasing injury risk.
IMT Standen is recalling certain leaf spring assemblies for trailers because they may crack and break, posing a road hazard and increasing crash risk.
Subaru is recalling 2019 Ascent vehicles because a faulty transmission sensor may cause loss of drive power and increase crash risk.
Subaru is recalling 51,613 2019 Crosstrek, Forester, and Ascent vehicles because a PCV valve can separate, causing loss of power and increasing crash risk.
REV Ambulance Group is recalling 2018-2019 Wheeled Coach Type 1 ambulances because oxygen tank brackets may loosen, posing an injury risk in crashes.
Piaggio is recalling 2020 Moto Guzzi V85 TT motorcycles because a final drive seal may leak oil onto the rear tire, increasing crash risk.
Altaire Pharmaceuticals is recalling Up & Up Intensive Relief Lubricating Eye Drops due to a lack of assurance of sterility.
Altaire Pharmaceuticals is recalling Equate Night & Day Restore Tears Lubricant Eye Pack due to a lack of assurance of sterility.
Altaire Pharmaceuticals is recalling ActivEyes Lubricant Eye Ointment due to a lack of assurance of sterility.
Altaire Pharmaceuticals is recalling Grandall Oftal-Mycin Ophthalmic Ointment because the product lacks assurance of sterility. The recall covers specific lots distributed nationwide.
Altaire Pharmaceuticals is recalling Equate Restore PM Nighttime Lubricant Eye Ointment because the product may not be sterile.
Altaire Pharmaceuticals is recalling Natural Ophthalmics Women's Tear Stimulation Dry Eye Drops due to a lack of assurance of sterility.