State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cordis Corporation is recalling 21 units of MAXI LD PTA Dilatation Catheters because they were manufactured using an expired inner body.
OrthoPediatrics Corp is recalling 969 Child Nail Attachment Bolts because they may bind with the intramedullary nail, potentially delaying surgical procedures.
OrthoPediatrics Corp is recalling 969 Adolescent Nail Attachment Bolts because binding between the bolt and nail may delay surgical procedures.
Mylan Pharmaceuticals is recalling 4,272 bottles of Prasugrel 5 mg tablets because they failed to meet dissolution specifications.
Keystone RV Company is recalling 2014 Springdale 253FWRLLS trailers because the Federal Identification Tag may list incorrect tire, rim, and axle sizes, potentially leading to unintentional overloading.
Sandoz Inc is recalling 76,644 bottles of Gatifloxacin Ophthalmic Solution 0.5% because the package insert is incorrect or missing.
Arbor Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because shipper cartons were mislabeled, potentially causing confusion with different vial sizes.
Sandoz Inc is recalling Bimatoprost Ophthalmic Solution 0.03% because the package insert is incorrect or missing. The recall covers 346,929 bottles distributed nationwide.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Nephron Pharmaceuticals is recalling 19,390 syringes of Succinylcholine Chloride Injection because of incorrect or missing lot and expiration dates.
AuroMedics Pharma LLC is recalling one lot of Ranitidine Tablets USP, 150 mg, because some bottles were found to be empty.
Sandoz Inc. is recalling 346,929 bottles of Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension due to incorrect or missing package inserts.
Merritt Manufacturing is recalling Angel Guard Angel Ride car beds because the restraint harness may not be properly sewn, increasing injury risk in a crash.
McElrath Trailers is recalling 2014-2019 VX trailers because side marker LED lights may lack required reflex reflectors, reducing visibility.
KZRV is recalling 2019-2020 Connect and Sportsmen trailers because optional Rock Run rear storage racks may detach when loaded, creating a road hazard.
Arcimoto is recalling 2019 FUV vehicles because a wiring defect may cause a loss of traction power, increasing the risk of a crash.
Cooper Europe is recalling specific Avon Cobra Chrome motorcycle tires because a thin innerliner may cause rapid deflation, increasing crash risk.
Daimler Trucks is recalling 2,725 Western Star 4900 and 5700 trucks because sleeper cab vent windows may detach due to improper adhesive.
Thor Motor Coach is recalling 2020 Sequence 20L motorhomes because solar panel screws may fail, causing the panel to detach and create a road hazard.
Forest River is recalling 2020 Cherokee Alpha Wolf travel trailers because an incorrectly connected wire may lack overcurrent protection, increasing the risk of fire.
Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because missing seat recliner parts may reduce occupant restraint in a crash.
Mercedes-Benz is recalling 24,226 vehicles due to a software fault that may cause the emergency call system to relay inaccurate location data, potentially delaying emergency responders.
Mercedes-Benz is recalling 29,720 vehicles because front seat belts may be incorrectly detected as unfastened, potentially disabling safety features.