State
73,576 recalls have nationwide distribution and so reach Alaska. 1,766 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,766 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 470 (27%) are Severe.
Which agencies issued them
These figures cover only the 1,766 recalls whose distribution notice names Alaska specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DeRoyal Industries is recalling Myocardial Probes that contain an 18mm needle instead of the specified 15mm needle.
Philips is recalling 611 MR 5300 MRI scanners due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
Philips is recalling Ingenia 3.0T and 3.0T CX MRI systems because a software issue can terminate examinations during image reconstruction if scan parameters exceed available system memory.
Fresenius Medical Care is recalling CombiSet Hemodialysis Blood Tubing Sets to ensure treatment preparation and handling steps are performed as instructed.
Philips is recalling 91 MRI systems due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Philips is recalling 922 Ingenia Ambition MRI systems due to a software issue that can terminate examinations if system memory is exceeded.
CooperVision is recalling specific lots of Pearle Vision 1 Day contact lenses because a small number of lenses have the incorrect power.
Ventec Life Systems is recalling two HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Philips is recalling 37 MR 7700 MRI systems due to a software issue that can terminate examinations during image reconstruction.
Philips is recalling 210 Achieva 3.0T MRI scanners because a software issue can terminate examinations if system memory is exceeded during image reconstruction.
Baxter Healthcare is recalling 169 PRO+ MRS Mattresses because UDI label errors may lead to incorrect product identification or use with incompatible bed frames.
Philips is recalling 82 Intera 1.5T MRI systems worldwide because a software issue can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Philips is recalling 2,038 Ingenia 1.5T MRI systems worldwide due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.
AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
Philips is recalling SmartPath MRI software due to a defect that can terminate examinations during image reconstruction if system memory is exceeded.
Philips is recalling 15 Achieva XR MRI systems because a software issue can terminate examinations if scan parameters exceed system memory.
Philips is recalling 596 Ingenia Elition MRI systems due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
WWF Operating Company is recalling So Delicious Dairy Free Salted Caramel Cluster Cashewmilk because it may contain small stones and other hard objects.
AVID Medical is recalling Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.
Ventec Life Systems is recalling 21 HomeFill Oxygen System cylinders because they lack required medical gas labeling.
Macleods Pharmaceuticals is recalling Olanzapine 5 mg tablets because organic and unspecified impurities exceeded specifications.
Chrysler is recalling MOPAR body and jumper wiring harnesses because water intrusion can disable electric power steering assist, increasing crash risk.
Rivian is recalling 2027 R2 vehicles because a high voltage battery fastener may be improperly tightened, which can cause a loss of drive power and increase crash risk.
Chrysler is recalling 2026 Ram 1500 vehicles because side air bag connectors may not be secured properly, potentially preventing deployment in a crash.