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.
ICU Medical is recalling 83 Cogent Hemodynamic Monitoring Systems due to software issues that may cause inaccurate data, unit shutdown, or loss of display.
Welch Allyn is recalling 78,521 Q-Tel RMS systems because they may not meet defibrillation withstand safety requirements.
GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel defect may cause the start button to stick, potentially leading to accidental radiation exposure.
Welch Allyn is recalling 78,521 ECG lead sets because they may not meet defibrillation withstand safety requirements.
Welch Allyn is recalling T12 wireless ECG devices because they may not meet defibrillation withstand safety requirements.
Elekta Inc is recalling 25 Leksell Vantage Stereotactic System Instrument Carriers because a faulty locking piece may not meet required locking force standards.
Welch Allyn is recalling S4 Wireless Telemeters and patient cables because they may not meet defibrillation withstand safety standards.
Welch Allyn is recalling Q-Stress and XScribe diagnostic devices because they may not meet specific defibrillation withstand safety requirements.
U&I Corp. is recalling 42 Velofix SA cervical cages because screw-hole dimensions may be out of range, posing a risk of screw pullout or instability.
Avanos Medical is recalling CORFLO Percutaneous Endoscopic Gastrostomy (PEG) Kits because the tube may become blocked at the adapter, potentially delaying or aborting procedures.
GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel issue may cause the start button to stick, potentially leading to accidental radiation exposure.
Merit Medical Systems is recalling PreludeSYNC Radial Compression Devices because inflatable balloons may break, causing air leakage and potential bleeding.
Welch Allyn is recalling 78,521 lead diagnostic electrocardiographs because they may not meet defibrillation withstand requirements.
Welch Allyn is recalling H12+ Holter Recorders and patient cables because they may not meet defibrillation withstand requirements.
Becton Dickinson is recalling 900 units of CareFusion Safe-T-Centesis Catheter Drainage Trays because the 8 Fr catheter was manufactured with a 6.9 Fr needle instead of the correct 8 Fr needle.
Smiths Medical ASD Inc. is recalling 100 units of Portex Lumbar Puncture Trays because the inner trays were mislabeled with an incorrect model number.
Siemens is recalling Atellica CH 930 Analyzers with specific software versions due to a defect that may cause incorrect test results.
Bio-Rad Labs is recalling 376 units of the Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test, Lot 18200A, due to elevated lot-to-lot bias affecting antibody measurements.
Obalon Therapeutics is recalling 45 Obalon Balloon Systems because the touchscreen may lose calibration, preventing balloon inflation.
Boston Scientific is recalling MoXy Laser Fibers to update instructions and reduce the likelihood of metal cap and fiber tip breakage.
Ortho Clinical Diagnostics is recalling VITROS TT4 Reagent Packs due to increased unsuccessful calibrations. The recall affects 3,181 units distributed in the US and 23 other countries.
Dr. Reddy's Laboratories is recalling 1,752 bottles of Esomeprazole Magnesium 40 mg capsules because the product contains brown pellets.
Daimler Trucks is recalling 2019 Freightliner Business Class M2 trucks because a wire harness connector may unplug, causing sudden loss of drive power and power steering.
Blue Bird is recalling 2018-2021 Vision buses with Ford 6.8L engines because parking brake cables may chafe fuel lines, creating a fire risk.
National Van Builders is recalling 2019-2020 Ford Transit and 2019 Ram Promaster vans because seat belt retractors may not secure occupants properly.