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.
Exactech is recalling 317 Optetrak Offset Tibial Trays because a design incompatibility exists with certain offset spine stiffener screws and constrained condylar tibial inserts.
Bugatti is recalling 2017-2018 Chiron vehicles because front seat recliner brackets may not be welded properly, which could cause the seat to move unexpectedly and increase crash risk.
Ford is recalling 2017 F-53 and F-59 chassis because missing plugs in the brake control unit may cause fluid leaks or air ingestion, increasing stopping distance.
Exactech, Inc. is recalling 520 Optetrak Constrained Condylar Offset Screws due to a design incompatibility with certain tibial inserts and trays.
Volkswagen is recalling 2018 Atlas vehicles because the fuel tank may have insufficient wall thickness, potentially causing a fuel leak and increasing fire risk.
Exactech is recalling 656 Optetrak Constrained Condylar Offset Screws due to a design incompatibility with certain tibial inserts and trays.
Exactech is recalling 606 Optetrak Constrained Condylar Offset Screws because they are incompatible with certain tibial inserts and trays.
Halyard Health is recalling specific lots of 15ml saline vials used in the Turbo-Cleaning Closed Suction System because they may leak, potentially exposing contents to infectious agents.
Exactech is recalling 643 Optetrak Constrained Condylar Offset Screws because they are incompatible with certain tibial inserts and trays.
Exactech, Inc. is recalling 306 Optetrak Offset Tibial Trays and Screws because a design incompatibility exists between certain screw sizes and tibial inserts.
Amerisource Health Services is recalling specific lots of Paroxetine tablets because they contain foreign tablets or capsules.
Exactech, Inc. is recalling 411 Optetrak Constrained Condylar Offset Screws due to a design incompatibility with certain tibial inserts and trays.
Shoreline Fruit is voluntarily recalling dark chocolate covered cherry products due to undeclared milk in the dark chocolate coating.
Medline Industries is recalling 1,428 Transfer/Gait Belts because the locking mechanism may fail to secure the strap, allowing it to slip through the buckle.
3M is recalling Bair Hugger temperature sensors because a programming error may cause the device to display a temperature lower than the patient's actual body temperature.
Exactech, Inc. is recalling 640 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Exactech is recalling 678 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain tibial inserts.
Exactech is recalling 889 Optetrak Constrained Condylar Offset Screws because they are incompatible with certain tibial inserts and trays.
Medline Industries is recalling 8,000 units of Sensicare Green Surgical Gloves because a possible open seal on the packaging could compromise sterility.
Exactech is recalling 920 Optetrak Constrained Condylar Offset Screws because they are incompatible with certain tibial inserts and trays.
Exactech is recalling 537 Optetrak Constrained Condylar Offset Screws due to a design incompatibility with certain tibial inserts and trays.
Exactech is recalling 207 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Exactech is recalling 311 Optetrak Offset Tibial Tray and Screws units due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.
Halyard Health is recalling Turbo-Cleaning Closed Suction Systems because saline vials may leak, potentially exposing contents to infectious agents.
Ford is recalling 2016 Explorer and F-150 vehicles because loose seat bolts may cause cushions to detach in a crash, increasing injury risk.