State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kar Nut Products Company is recalling Kar's Sweet n' Salty Mix 34 oz. bags due to the possibility of very small pieces of glass in the product.
Civco Medical Instruments is recalling PercuNav tracking bracket kits because the sterility of the product cannot be assured.
Ameditech is recalling Micro Screen 6 Panel Cup drug abuse tests because they have shown reduced reactivity.
Philips is recalling ECG sync cables used with HeartStart monitors because electrical interference can cause misinterpretation of heart signals or interrupt pacing.
Columbia Northwest is recalling 2013-2014 Somerset E1 and Santa Fe trailers because the water heater may overheat, causing scalding.
National Frozen Foods is recalling Target-exclusive Italian Blend frozen vegetables due to potential Listeria monocytogenes contamination.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Lakeside Foods is recalling specific lots of frozen peas and carrots after testing confirmed the presence of Listeria monocytogenes.
Forest River is recalling specific 2007-2015 motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.
National Frozen Foods Corporation is recalling Monarch and Valmont Italian Vegetable Blend due to potential Listeria monocytogenes contamination.
Precision Medical is recalling 315 Easy Dial Oxygen Regulators because the settings label may be off by one position, causing incorrect oxygen flow.
Downing Labs, LLC is recalling Taurine Injectable, 50mg/mL, 30mL vials due to a lack of assurance of sterility. The recall affects 123 vials distributed nationwide and internationally.
Civco Medical Instruments is recalling 54 boxes of Large Gauge Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Kar Nut Products Company is recalling Kar's Sweet n' Salty Mix because the product may contain very small pieces of glass.
National Frozen Foods Corporation is recalling frozen Italian Vegetable Blend due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Civco Medical Instruments is recalling 717 boxes of Infiniti Plus Needle Guides because the sterility of the product cannot be assured.
Kar Nut Products Company is recalling 140,322 bags of Kar's Sweet n' Salty Mix due to the possibility that the product may contain very small pieces of glass.
Civco Medical Instruments is recalling 1,139 boxes of Biopsy Starter Kits because the sterility of the product cannot be assured.
Newmar is recalling 2016 King Aire vehicles that may lack a required emergency exit window over the driver's side dinette table, potentially delaying escape during an emergency.
US Compounding Inc is recalling 1,421 vials of Lincomycin/Lidocaine due to deficient practices that may impact sterility assurance.
TZ Medical Inc. is recalling Neptune Plus hemostasis pads because the instructions for use do not match the original FDA submission.
Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.
Ameditech is recalling specific Immutest drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and in Australia.
Ameditech is recalling 787 kits of 1 Step 12 Panel Cup drug tests due to reduced reactivity. The products were distributed in the US and Australia.
Ameditech is recalling iCup drug screen cups because they have shown reduced reactivity. The affected units were distributed nationwide in the US and internationally to Australia.