State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Herbal Doctor Remedies is recalling Lump Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Herbal Doctor Remedies is recalling Fungo Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Randox Laboratories is recalling Human Assayed Multi-Sera Level 2 controls due to incorrectly assigned target and range values for specific analytes.
Herbal Doctor Remedies is recalling Deafness Off Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Siemens Medical Solutions is recalling two Lantis 6.1 Commander units due to a Microsoft Windows Remote Desktop Protocol vulnerability.
Philips is recalling 26 Vereos PET/CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.
Geistlich Pharma is recalling Bio-Oss Pen applicators because a visible piece of green plastic was found on the outer barrel when unscrewing the cap.
Unipharma is recalling CVS Health Children's Allergy Relief Liquid Medication due to potential contamination with B. cepacia bacteria. The recall is a precautionary measure.
Philips is recalling Ingenuity Core CT systems because images may be incorrectly labeled as having phase tolerance applied when it was not.
Herbal Doctor Remedies is recalling Hair Back 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Philips is recalling EPIQ and Affiniti ultrasound systems with software version 4.0 because patient images may be moved to the wrong folder.
Herbal Doctor Remedies is recalling Thyro-Lo 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Ortho Clinical Diagnostics is recalling 2,531 VITROS 5600 Integrated Systems due to a software anomaly that may cause unsuccessful calibration.
Herbal Doctor Remedies is recalling Asma Stopper Capsules because they were manufactured outside of current Good Manufacturing Practice controls.
Polymer Technology Systems is recalling 559 vials of IVD Lipid Panel test strips because the accompanying MEMo chips may be mislabeled, potentially causing the analyzer to display the wrong lot number.
Polymer Technology Systems is recalling Lipid Panel test strips because the included MEMo chips may display the wrong lot number on the analyzer screen.
Sage Products Inc is voluntarily recalling a lot of Independent Care System kits because the included Sodium Bicarbonate Mouthpaste tubes may be cosmetically damaged.
SunSetter is recalling vinyl covers for motorized awnings because they can cause unexpected opening and falls. One death and six injuries have been reported.
Tiffin is recalling 2019-2020 Allegro Open Road motorhomes because a hydraulic hose may rub against the tire, causing sudden deflation and crash risk.
E-One is recalling 2019 Cyclone II and Typhoon fire trucks because air bag cushions may detach and fail to inflate during a crash.
Kia is recalling 2020 Telluride vehicles because seat belt assemblies may not securely hold child restraints in a crash, increasing injury risk.
VanLeigh is recalling 2015-2019 Beacon and Vilano fifth wheel trailers because short suspension shackles may fail, increasing crash risk.
Mercedes-Benz is recalling 2020 GLE and GLS vehicles because incorrectly installed air conditioner drain hoses may cause water to enter the cabin, increasing the risk of fire.
Ford is recalling 2015 Fusion and Lincoln MKZ vehicles because heat from seat belt pretensioners may cause anchor cables to fail, increasing injury risk in crashes.
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because the rear middle seatbelt anchor may be loose, increasing injury risk in a crash.