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.
Trader Joe's is recalling Imported English Authentic Lemon Curd because it contains undeclared milk in the butter ingredient.
Nu Skin Enterprises is voluntarily recalling Pharmanex BioGinkgo tablets because they contain undeclared wheat, a major food allergen.
Mako Surgical Corporation is recalling 777 MAKO RIO THA Application User Guides because five AFMEA Risk Control Measures are missing from the documents.
Remel Inc is recalling Haemophilus Test Medium agar plates because poor organism growth may result in incorrect susceptibility test results.
Actavis Inc is recalling specific lots of Levofloxacin Ophthalmic Solution because the product failed impurity specifications for a related compound.
Teva Pharmaceuticals is recalling Risedronate Sodium Delayed-release Tablets because stability testing revealed low out-of-specification dissolution results.
Metrex Research is recalling CaviWipes Extra Large surface disinfectants because they may have been contaminated during the packaging process.
LEO Pharma is recalling 272,062 tubes of Calcipotriene Cream because the label omitted a required excipient and a warning about contact dermatitis.
Merge Healthcare is recalling Merge Cardio software versions 9.0 and 10.0 because measurements from images or US carts do not transfer to reports in the correct unit of measure.
Siemens is recalling nine Biograph Mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population of devices.
Merge Healthcare is recalling specific versions of Merge PACS software because studies may fail to propagate or import via the telmed protocol.
Siemens is recalling 18 Biograph 6 TruePoint mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population.
Siemens is recalling four Biograph Mobile PET/CT units because specific mobile instructions were not shipped to a limited population.
Sandoz Inc is recalling specific lots of Pioglitazone and Glimepiride Tablets because they failed to meet dissolution specifications.
Siemens Healthcare Diagnostics is recalling Dimension Vista LOCI Progesterone tests because DHEA-S causes falsely elevated results.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Progesterone tests because DHEA-S causes falsely elevated results.
Siemens Medical Solutions is recalling six Biograph Mobile PET/CT units because mobile-specific instructions were not shipped to a limited population of systems.
Integra LifeSciences Corp. is recalling 39 units of the UNI-CP System due to incorrect labeling on the plate.
US Endoscopy Group Inc is recalling Roth Net Polyp Retrieval devices because the expiration date on the outer carton is shorter than the date on the inner package.
Navistar is recalling 2016-2018 International heavy diesel trucks because a mounting bracket may fracture, causing air leaks and increased stopping distance.
Mercedes-Benz is recalling 2016 G550 and G63 vehicles because a door cable may break, preventing occupants from opening the door from inside after a crash.
Altec is recalling 2015-2016 Aerial Devices and Service Body Trucks due to a wiring defect that may cause a short circuit and increase fire risk.
Volvo Bus is recalling 2016-2017 9700 transit buses because a ground cable may be improperly installed, causing the engine to stall unexpectedly.
Jayco is recalling 2017 Designer fifth wheel trailers because the spare tire rim may rub against the brake caliper, increasing crash risk.
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because the Federal Placard incorrectly lists axle capacity as 5,000 lbs instead of 4,000 lbs.