State
73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Noven Pharmaceuticals is recalling Estradiol Transdermal Systems because the adhesive may not stick well to the skin.
Stryker is recalling 321 units of DirectInject bone cement because the paste cannot be injected from the syringe into the target location.
Heartware, Inc. is recalling Instructions for Use and Patient Manuals for the HeartWare HVAD System to update guidance on intermittent alarm issues.
Noven Pharmaceuticals is recalling Minivelle estradiol transdermal patches because the adhesive may not stick well to the skin.
Medtronic is recalling 11 Endoskeleton TC Interbody System devices because shelf boxes were mislabeled, containing the wrong size device.
C.R. Bard is recalling 9,800 units of Bard Clean-Cath Intermittent Catheters because the catheter tip was cut off and the packaging was not fully sealed.
Azure Biotech Inc. is recalling 100,000 Assure COVID-19 IgG/IgM Rapid Test Devices due to incorrect diagnostic labeling and unsupported expiration dating.
Medtronic is recalling 11 Endoskeleton TC Interbody System devices because shelf boxes misidentify the size of the contained device.
Welch Allyn is recalling 213 Surveyor S12/S19 Bedside Patient Monitors because they do not meet IEC 60601-2-27 safety requirements as labeled.
Welch Allyn Inc Mortara is recalling 27 ELI 380 Electrocardiographs because they do not meet IEC 60601-2-27 requirements as labeled.
Edge Pharma is recalling 5,850 syringes of Betadine ophthalmic solution because a defective container may compromise sterility. The product is distributed nationwide.
Heartware, Inc. is recalling Instructions for Use and Patient Manuals for the HVAD System to correct inaccurate descriptions of controller connection verification.
Mitsubishi Fuso is recalling 2019-2021 FEC7T trucks because the rear leaf spring may break, creating a road hazard and increasing crash risk.
Audi is recalling certain 2019-2021 vehicles for rear axle lock nuts that may break from stress corrosion. A broken lock nut can cause axle misalignment, loss of control, and increased crash risk.
Mack Trucks is recalling 2019-2020 LR vehicles because the steering transfer case may have insufficient oil, which can cause steering lock-up and increase crash risk.
Keystone is recalling specific 2021 Passport trailers because the installed safety chains are underrated for the vehicle's weight rating, which could allow the trailer to detach from the tow vehicle.
LGS Industries is recalling 2021 LOOK, Pace, and Cargo Express trailers because an axle bracket may separate, affecting stability and increasing crash risk.
More Than Gourmet is recalling beef and veal broth products that may contain hydraulic oil. No illnesses have been reported.
Mercedes-Benz is recalling certain 2020-2021 GLE and GLS vehicles because incorrectly installed air conditioner drain hoses may cause water intrusion, leading to electrical short circuits and fire.
Super World Trading Inc. is recalling approximately 26,270 pounds of ready-to-eat fish chips imported from China because the country is ineligible to export processed products to the U.S.
Forest River is recalling 2021 Coachmen Catalina travel trailers because an incorrectly gauged battery wire may melt and cause a fire.
REV Ambulance Group Orlando is recalling 2019-2021 Type I and IX ambulances because LCD displays may lock up, potentially delaying emergency efforts.
Rosenbauer America is recalling specific fire trucks because rear lights may be too bright, potentially blinding other drivers and increasing crash risk.
Gillig is recalling 229 CNG-powered buses because insufficient roof door overlap may allow accidental opening, increasing crash risk.
Blue Bird is recalling 2020-2022 Vision and All American school buses because a check valve may fail to isolate air, potentially causing unintended spring brake application and increasing crash risk.