State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2020 Escape vehicles because the Body Control Module may fail to detect low tire pressure, increasing crash risk.
Peloton is recalling PR70P clip-in pedals fitted on bikes sold between July 2013 and May 2016 because they can break unexpectedly, causing laceration injuries.
Genie is recalling 2020 TZ-34 and TZ-50 trailer-mounted boom lifts because under-tightened bolts may affect stability and increase injury risk.
Sales BSD is recalling Homerygardens extension cord splitters because the wire size cannot handle the appropriate amp load, posing a fire hazard.
Biomet is recalling OnPoint Scope Procedure Kits because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.
Roche Diagnostics is recalling BenchMark ULTRA Advanced Staining Systems due to a risk of fluid leaks causing electrical shorts, heat, and fire.
Daimler Vans USA is recalling 2020 Mercedes-Benz Sprinter vans because damaged brake hoses may leak fluid, increasing crash risk.
Roche Diagnostics is recalling the DISCOVERY ULTRA Advanced Staining System due to fluid leaks that can cause electrical shorts, heat, and smoke.
Bombardier is recalling 2020 Can-Am Ryker motorcycles because improperly installed front wheels may separate, increasing crash risk.
AB ULAX is recalling 1500 Flex Heat and Moisture Exchangers because they may disconnect from the respiratory circuit, potentially causing hypoxia or death.
Biomet is recalling Regenerex Primary Taper Caps because they were not properly aligned for gamma sterilization, potentially leaving them unsterilized.
Toyota is recalling 2020 Highlander and Highlander Hybrid vehicles because incorrect seat trim covers may prevent side airbags from deploying properly, increasing injury risk in a crash.
Encore Medical is recalling 190 units of DJO EMPOWR Tibial Knee Punch Handles because the retaining pin may fall out, potentially leaving debris in the joint space.
Medline Industries is recalling 16 non-sterile Left Heart Kits sold to facilities without sterilization capabilities. The kits were intended to be sterilized prior to use.
Biomet is recalling ARTHROSIMPLICITY KIT EU units because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.
Daimler Trucks North America is recalling approximately 53 units of 2020-2021 Western Star and Freightliner commercial trucks due to incorrect Gross Axle Weight Rating information on vehicle certification labels. This could lead to axle overloading and increased crash risk.
Biomet, Inc. is recalling ONPOINT SCOPE PROCEDURE KIT-EU units because they were not properly aligned with the gamma sterilization group, resulting in improper sterilization.
Medline Industries is recalling 80 non-sterile vascular surgery kits sold to accounts without sterilization capabilities. The kits were distributed nationwide, including in CA, CO, CT, OH, TX, and NY.
Ansell Healthcare Products LLC is recalling Microflex Diamond Grip Examination Gloves because they were shipped without verification of barrier integrity.
Medline is recalling 80 non-sterile MTO Protection Station Plus kits because they were sold to facilities without sterilization capabilities.
Medline is recalling 16 non-sterile left heart kits sold to accounts without sterilization capabilities. The kits require sterilization prior to use.
Medline Industries is recalling 20 non-sterile radiology kits that were sold to accounts without the ability to sterilize them prior to use.
Medline Industries is recalling 60 non-sterile Left Heart Kits sold to accounts without sterilization capabilities. The kits were distributed nationwide.
Medline Industries is recalling 32 non-sterile cath lab kits because they were sold to accounts without the capability to sterilize them prior to use.
Nuvasive is recalling 41 Precice Bone Transport System units because standard removal tools can cause the distal plug to disassociate during explantation.