State
73,576 recalls have nationwide distribution and so reach Minnesota. 7,844 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,844 recalls naming Minnesota we have scored against our rubric, 1,139 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,243 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,844 recalls whose distribution notice names Minnesota specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Howmedica Osteonics Corp. is recalling specific Scorpio knee implant components due to aged polyethylene material that may cause increased wear and potential device failure.
Jaguar Land Rover is recalling one 2026 Range Rover Sport because a misaligned circuit board in the powertrain control module may cause loss of drive power.
NOXBOX LTD is recalling 1,547 NOxBOXi Nitric Oxide Delivery Systems due to potential oxygen tubing leaks that may cause oxygen desaturation.
Stryker is recalling 9,072 XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Maquet Cardiopulmonary GmbH is recalling Percutaneous Insertion Kits because packaging may not consistently maintain sterile barrier integrity.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Datex-Ohmeda is recalling 140 Aisys CS2 anesthesia systems because electronic gas mixer assemblies may fail, interrupting anesthetic delivery and requiring clinician intervention.
Forest River is recalling 2026-2027 Dynamax Isata recreational vehicles because a misaligned bunk mat may not be supported, increasing the risk of occupant injury.
Medical Action Industries is recalling blood culture kits containing BD ChloraPrep applicators with potentially compromised sterile seals, posing a risk of localized skin infection.
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.
Tiffany Food Corp is recalling Hexing Haw Balls candy because it contains the unapproved dye Ponceau 4R.
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.