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.
Datex-Ohmeda is recalling seven Aisys CS2 anesthesia systems because a gas mixer defect can interrupt anesthetic delivery, requiring clinician intervention to prevent decreased patient effect.
Medline Industries is recalling 336 cataract convenience kits because open sterile seals may compromise sterility and lead to patient infection.
Forest River is recalling 2026-2027 Dynamax Isata recreational vehicles because the bunk ladder may loosen if attached to a wooden mattress insert, increasing injury risk.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
F & A Foundation is recalling 600 units of Reign Medical Clench Staple Systems because the device's performance characteristics have not been adequately established.
Taro Pharmaceuticals is recalling Lidocaine Ointment 5% due to failed content uniformity specifications during stability testing.
Wilson-Cook Medical Inc. is recalling 121,241 units of Hemospray Endoscopic Hemostat due to issues with endoscope adherence and the inability to spray powder.
Straumann USA LLC is recalling 216 GM Helix Implants because the packaging identification does not match the actual implant dimensions.
Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.
Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product is distributed nationwide.
ICU Medical is recalling IV Non-Dedicated Gravity Administration Sets because black specks in the drip chamber may cause healthcare providers to delay therapy.
Embecta Medical II LLC is recalling pen needles labeled 'For Investigational Use Only' that were inadvertently distributed as commercially marketed devices.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide.
ICU Medical is recalling 107,800 oncology sets because drip chambers may contain black specks from the molding process, which could lead to product replacement and therapy delays.
Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product was distributed nationwide in the USA.
ICU Medical is recalling 28,550 oncology sets because drip chambers may contain black specks from the molding process. The discolored material does not enter the fluid path but may cause therapy delays.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide in the USA.
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.
Inventia Healthcare Limited is recalling 13,567 bottles of Chlorthalidone 25 mg tablets because they failed dissolution specifications. The recall is nationwide.
Star Meat Delivery Inc. is recalling raw pork, beef, and goat products produced without federal inspection and bearing false USDA marks.
Nova Bus is recalling 2024-2025 LFS transit buses because an improperly tightened emergency brake valve may cause air leaks and unintentional parking brake activation.
Ford is recalling 2024-2026 Ranger vehicles with 10.1-inch center stack screens that may lose power and fail to display the rearview camera image, increasing crash risk.
Ford is recalling specific 2025-2027 Expedition and F-Series Super Duty vehicles because contaminated LED chips in the headlights may cause a loss of exterior lighting, increasing crash risk.