State
73,741 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,849 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 2,245 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2019 Jeep Cherokee vehicles because loose front passenger seat mounting bolts may allow the seat to move in a crash, increasing injury risk.
Royale is recalling 2015-2017 Mercedes Sprinter-based mini coaches because the rear seat cushion may not stay locked in place during a crash or sudden stop.
Honda is recalling 2014-2019 Acura MDX and 2017-2019 MDX Sport Hybrid vehicles because moisture may enter the tailgate lid lights, causing them to fail and reducing vehicle visibility.
Fire Equipment Sales & Service is recalling two 2018 emergency vehicles because their brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Royale is recalling 2015-2018 Ford Transit-based mini-coaches because the back seat cushion may not stay locked in place during a crash or sudden stop.
Blanchat is recalling one 2018 B-27 Minuteman vehicle built on a Ford F-550 chassis because the brake lights may illuminate without the brake pedal being pressed.
Midwest-CBK is recalling Baby Rattle Socks because small ornaments can detach, posing a choking hazard to young children. No injuries have been reported.
REV Ambulance Group is recalling 2018-2019 Road Rescue Ultramedic vehicles because backup camera displays may revert to factory settings, causing the image to reverse.
Blanchat Mfg. is recalling one 2018 B-27 Minuteman vehicle built on a RAM 5500 chassis because the brake lights may illuminate without the brake pedal being pressed.
Interline Brands is recalling ProPlus Brass Flare Swivel Fittings because they can leak, posing a fire hazard. Consumers should contact Interline for a full refund or replacement.
Chrysler is recalling 2019 Dodge Chargers because the sun visors may lack required air bag warning information, increasing the risk of injury.
Camber Pharmaceuticals is recalling Losartan Potassium tablets because trace amounts of the nitrosamine NMBA were detected in the active ingredient.
Advanced Pharma Inc. is recalling 140 syringes of Glycopyrrolate 0.6 mg/3 mL Injectable Solution because the company cannot ensure the product is sterile.
Advanced Pharma Inc. is recalling 1,850 syringes of Phenylephrine HCl Injectable Solution nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling 360 bags of fentanyl injectable solution nationwide due to a lack of assurance of sterility.
AvKARE Inc. is recalling Losartan Potassium and Hydrochlorothiazide Tablets because an impurity, N-Methylnitrosobutyric acid (NMBA), was identified.
Advanced Pharma Inc. is recalling 1,125 bags of Midazolam Injectable Solution nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling 2,400 syringes of Hydromorphone HCl injectable solution nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling 2,325 syringes of Morphine Sulfate 30 mg/30 mL Injectable Solution nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling 800 syringes of Phenylephrine HCl Injectable Solution due to a lack of assurance of sterility. The product was distributed nationwide.
American Health Packaging is recalling Valsartan Tablets 160 mg because a carcinogenic impurity was detected in the active ingredient.
Advanced Pharma Inc. is recalling 5,700 syringes of Neostigmine Methylsulfate Injection Solution because there is a lack of assurance of sterility.
Camber Pharmaceuticals is recalling Losartan Potassium tablets because trace amounts of the impurity NMBA were detected in the active ingredient.
AvKARE Inc. is recalling Losartan Potassium and Hydrochlorothiazide Tablets because an impurity, N-Methylnitrosobutyric acid (NMBA), was identified.
Advanced Pharma Inc. is recalling 550 syringes of Esmolol HCl Injectable Solution due to a lack of assurance of sterility. The affected products were distributed nationwide.