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.
Nissan is recalling approximately 24,793 2021 Rogue vehicles due to abnormal wear in the fuel pump that may cause overheating, failure, and engine stall, increasing crash risk.
Prevost is recalling 2020-2022 X3 Commuter and X3 Coach buses because the front ceiling panel may fall, posing a crash or injury risk.
Autocar is recalling 2019-2022 Xpeditor and 2020-2022 Legend vehicles. Fuel tubes may crack, causing a high-pressure leak that could ignite in the presence of a fire source.
Onions 52 is recalling 40-pound cartons of Jumbo Yellow Onions imported from Chihuahua, Mexico, due to possible contamination with Salmonella Oranienburg. The recall is voluntary and covers products distributed nationwide and in select regions.
Pfizer is recalling one lot of 5% Dextrose Injection (50 mL ADD-Vantage Units) due to lack of sterility assurance; the bags have the potential to leak. This is a Class II recall affecting 765 bags distributed nationwide.
Daimler Trucks North America is recalling 2021-2022 Western Star 4900 vehicles because the steering shaft pinch bolt may not be properly tightened, risking loss of steering control.
Onions 52 is voluntarily recalling 5-pound cartons of Jumbo Red Onions labeled Imperial Fresh due to possible Salmonella Oranienburg contamination. The onions were imported from Chihuahua, Mexico and distributed nationwide.
Daimler Trucks North America is recalling 2022 Thomas Built SAF-T-LINER C2 school buses because the gas pedal assembly may be misaligned and wear through the floor mat, potentially trapping the pedal and causing unintended acceleration.
Sandoz Inc. is recalling 45,036 cartons of Enoxaparin Sodium Injection USP 40 mg/0.4 mL due to temperature abuse during shipping. The affected lot was distributed nationwide.
Onions 52 is voluntarily recalling Medium Red Onions imported from Chihuahua, Mexico due to possible contamination with Salmonella Oranienburg. The affected products were distributed nationwide.
Volkswagen Group of America (Audi) is recalling certain 2018–2022 Audi Q5 and SQ5 vehicles. Water or liquid can seep into the gateway control module, causing sudden engine power loss and increasing crash risk.
Mark of Fifth Avenue children's robes do not meet federal flammability standards for sleepwear and pose a risk of burn injuries. About 10,000 units sold online at Amazon and Walmart from August 2019 through June 2021 are affected.
Boston Scientific is recalling Hurricane RX dilation balloons used in endoscopic biliary procedures due to pinhole defects causing pressure loss that may prolong treatment.
Boston Scientific is recalling Hurricane RX Dilation Balloons nationwide due to pinhole defects that cause pressure loss or failure to maintain pressure during endoscopic procedures.
Siemens is recalling 1,326 Dimension Vista 500 diagnostic devices worldwide due to incorrect default hemolysis, icterus, and lipemia indices that may affect test result accuracy.
Wright Medical Technology is recalling INBONE Total Ankle System implants because the package contents and package labeling do not match.
Boston Scientific is recalling specific lots of Hurricane RX Dilation Balloons due to a pinhole defect that causes pressure loss, resulting in prolonged endoscopic procedures. Affected devices are used for dilating strictures in the bile duct.
Boston Scientific is recalling the Hurricane RX Dilation Balloon due to a pinhole defect causing pressure loss during endoscopic procedures. The defect may result in prolonged procedures and inability to effectively treat biliary strictures.
Siemens is recalling 1,407 Dimension Vista 1500 diagnostic devices worldwide due to incorrect default Hemolysis, Icterus, and Lipemia (HIL) index values affecting five assays.
MAX LUX CORP is recalling approximately 9900 handheld UV-C germicidal wands (Safe-T Lite) distributed nationwide due to excessive ultraviolet-C radiation emissions.
Target Good & Gather Mixed Berry Sparkling Water in 8-packs is being recalled due to unlabeled sulfites. Keurig Dr Pepper discovered the issue after receiving complaints about off flavor and off aroma.
GE Appliances is recalling approximately 132,000 free-standing and slide-in electric and gas ranges because they can tip over if a heavy object is placed on an open oven door and the anti-tip-over bracket is not securely installed, risking burn injuries.
Boston Scientific is recalling HURRICANE RX Dilation Balloons due to a pinhole defect that causes pressure loss during endoscopic procedures. The device may fail to maintain necessary pressure, potentially prolonging procedures.
Keurig Dr Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water because some cans contain unlabeled sulfites. The affected products were distributed nationwide.
BioFire Blood Culture Identification 2 (BCID2) diagnostic panels are being recalled due to increased risk of false positive Acinetobacter calcoaceticus-baumannii results caused by non-viable contamination in blood culture vials.