State
73,809 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Respire Medical is recalling the Respire Pink H/S Oral Sleep Apnea Device due to a potential for device breakage during use.
Arrow International is recalling 416,055 Maximal Barrier Drapes because unsealed packaging may compromise product sterility. The recall covers lots distributed in the US and 34 other countries.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Genesee BioMedical is recalling 444 Sternal Valve Retractors used in cardiac surgery due to corrosion that may cause the bearing or button to break.
Arrow International Inc. is recalling ARROWg+ard Blue Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling 416,055 Clear Fenestrated Drapes with Adhesive because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 Two-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International Inc. is recalling 416,055 Maximal Barrier Drapes because unsealed packaging may compromise product sterility.
Respire Medical is recalling 25 units of the Pink+ Hard Oral Sleep Apnea Device due to a potential for device breakage during use.
Arrow International Inc is recalling 7Fr. Catheter Clamps with Fastener because unsealed packaging may compromise product sterility.
Arrow International is recalling Radial Artery Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling VPS Rhythm ECG Accessory Packs because unsealed packaging may compromise product sterility. The recall affects 416,055 units distributed in the US and 35 other countries.
Morski Brands Inc. is recalling Finest Traditions Deluxe Potato Salad due to potential Listeria monocytogenes contamination. The product was distributed in six states.
Arrow International is recalling Spring Wire Guide Introducer Needles because unsealed packaging may compromise product sterility.
Ad-Tech Medical Instrument Corporation is recalling 30 sterile Disposable Drill Kits because they may contain drill bits from the wrong catalog number.
Morski Brands Inc. is recalling Terry's Potato Salad due to potential Listeria monocytogenes contamination. The product was distributed in six states.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Respire Medical is recalling the Pink Series EF+ Oral Sleep Apnea Device because it may break during use.
Arrow International is recalling 416,055 PICC Catheter Trimmers because unsealed packaging may compromise product sterility. The recall covers units distributed in the US and 34 other countries.
Spartan Motors is recalling 1991-2018 Utilimaster Aeromaster and Walk-In Vans because front seat belts lack required retractors, increasing crash injury risk.
Arrow International is recalling Maximal Barrier Drapes because unsealed packaging may compromise product sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International is recalling SnapLock Catheter/Syringe Adapters because unsealed packaging may compromise sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International is recalling 416,055 two-lumen central venous catheterization kits because unsealed packaging may compromise product sterility.
Arrow International is recalling specific lots of ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kits because unsealed packaging may compromise sterility.