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.
Nova Biomedical is recalling StatStrip Glucose meters due to a software defect that may assign patient test results to the wrong medical record.
Abiomed is recalling 1,422 Impella Optical Controllers because a purge flag component may fail, causing purge cassette recognition issues.
Forest River is recalling 2025-2026 Cedar Creek fifth wheel trailers because a sleeper sofa may block the bunkroom door, potentially delaying emergency exits.
Medline Industries is recalling 341 anesthesia pain kits due to open sterile seals that may compromise sterility and lead to patient infection.
Howmedica is recalling specific orthopaedic implant components made with aged UHMWPE material that may oxidize, potentially leading to increased wear and device failure.
ICU Medical is recalling Plum administration sets because drip chambers may contain black specks or discolored PVC material. The presence of particulate matter in the fluid path has not been ruled out.
Datex-Ohmeda is recalling 410 Et Control software units for anesthesia gas machines that may interrupt anesthetic delivery, requiring clinician intervention to prevent decreased patient effect.
Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity, posing a risk of infection.
Medline Industries is recalling 459 units of Minor Pack convenience kits because open sterile seals may compromise sterility and lead to patient infection.
Medline is recalling 135 Open Heart A Pack kits in California due to a potential sterile barrier breach in the RCSP cannulae, posing a risk of infection.
Happiest Baby, Inc is recalling 1,055 units of SNOO Sleep Sacks because Extra Small and Extra Large sizes have not been reviewed for safety and effectiveness by the FDA.
Howmedica is recalling Triathlon hinge inserts made with aged polyethylene that may wear excessively, potentially causing device fracture or the need for revision surgery.
Nuclein LLC is recalling 182 DASH Rapid PCR Instruments due to a software issue. The recall affects units distributed in 18 US states.
GE Healthcare is recalling Workflow Core Services V8 because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
GE Healthcare is recalling Core Services Hub V8 software because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
Happiest Baby, Inc. is recalling SNOO Sleep Sacks because they have not been reviewed for safety and effectiveness by the FDA.
Mirion Technologies is recalling 783 Captus 4000e Thyroid Uptake Systems because a tension bolt may fail, causing the spring arm to fall unexpectedly.
ICU Medical is recalling 185,688 CADD Yellow Medication Cassette Reservoirs because they may leak medication at the connector joint, potentially interrupting therapy or causing exposure to harmful agents.
Embecta Medical II LLC is recalling Nano Pro Un-Cannulated Demo Samples because investigational-use-only pen needles were inadvertently distributed as commercially marketed devices.
Datex-Ohmeda is recalling Aisys anesthesia systems because electronic gas mixer assemblies may fail, interrupting anesthetic delivery and requiring clinician intervention.
Bayer Medical Care is recalling 27,800 Stellant FLEX Syringe Kits because some may not have been properly sterilized due to a manufacturing issue.
GE Healthcare is recalling Enterprise Archive V8 software because historical imaging data may be incorrectly associated with different patients, potentially leading to misdiagnosis.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Philips North America is recalling 312 units of the PIC iX Essentials patient information system due to a software malfunction that may cause the system to freeze.