State
73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sun Pharmaceutical recalls CEQUA cyclosporine ophthalmic solution nationwide due to low assay results and particulate matter found in specific lots.
Brius Technologies recalls Brius Pontics custom orthodontic devices that were sold before completing required design control procedures and documentation.
Cook Medical recalled 24,641 Gunther Tulip Vena Cava Filter Sets due to updates required in the Instruction for Use documentation covering device description, indications, contraindications, warnings, and precautions.
Jubilant Cadista Pharmaceuticals is recalling Methylprednisolone Tablets USP 4mg because they contain less active ingredient than labeled. Lot 21 P0322 was distributed nationwide and in Puerto Rico.
SA3, LLC is recalling Silatrix Oral Gel Polymerized Sucralfate Gel due to failed microbial testing. Consumers should not use the product and contact their healthcare provider or SA3, LLC.
Brius Technologies is recalling Brius Patient Specific Brackets that were sold before the company completed the required design control process and regulatory documentation.
Pfizer is recalling quinapril and hydrochlorothiazide tablets (20 mg/25 mg) nationwide due to elevated chemical impurities exceeding acceptable daily intake limits. No illnesses have been reported.
The YSIO X.Pree x-ray system's user interface displays incorrect collimation information during image acquisition. While actual collimation functions correctly, the display does not match preset parameters, potentially confusing operators.
The Natural Dentist Healthy Breath Antiseptic Rinse (Cool Mint) is being recalled due to a label mix-up. The back label incorrectly states the active ingredient as Peppermint Oil and Sage Oil and displays the wrong UPC code.
Ritedose is recalling 3,795 prefilled syringes of sodium chloride injection nationwide. The barcodes incorrectly identify the product as rocuronium bromide, creating a medication identification risk in healthcare settings.
Cook Medical is recalling Celect Platinum Vena Cava Filter Sets due to revisions needed in the instructions for use, including updates to contraindications, warnings, precautions, and potential adverse events.
Tesla is recalling certain 2020-2022 Model S, X, Y and 2017-2022 Model 3 vehicles. The Boombox feature can obscure Pedestrian Warning System sounds while driving. A free software update will disable Boombox in Drive, Neutral, and Reverse modes.
Prevost is recalling 2021-2022 X3-45 Commuter buses because improperly tightened seat frame bolts may allow seats to move during a crash.
Prevost is recalling 2018 X3-45 buses because frayed seat belt wires may prevent buckles from working properly, increasing injury risk in crashes.
Newmar is recalling multiple 2019–2022 RV models due to unsecured wiring beneath seats that can cause electrical short circuits and fire. Owners should contact their dealer for free inspection and repair.
Tesla is recalling certain 2021-2022 Model X vehicles due to a defect in the left or right front-row side curtain air bags that may not deploy properly when windows are lowered. Improper deployment increases the risk of injury during crashes.
Big Tex Trailer Manufacturing is recalling 2022 50SR and 70SR trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.
Mercedes-Benz is recalling 21,306 vehicles because a ground cable bolt may not be secured properly, which can cause the electrical cable to overheat and increase the risk of a fire.
Columbus Trading-Partners USA is recalling CYBEX Sirona M child seats because loose foam pieces from the headrest pad may pose a choking hazard to children.
Mercedes-Benz is recalling 126,443 vehicles from 2018-2021 because the rearview camera display may fail to show the rear view due to a software error, reducing visibility and increasing crash risk.
Daimler Trucks North America is recalling certain 2020-2022 Western Star 49X and 2021 Western Star 47X vehicles because windshield wiper linkages may break, causing wipers to fail and reducing visibility.
Bestar wall beds can detach from the wall and fall, creating impact and crush hazards. One death and 60 additional injuries have been reported.
Hyundai is recalling 2019 Nexo vehicles because a filter may detach after refueling, causing a hydrogen leak that could lead to fire.
Daimler Trucks North America is recalling certain 2020-2023 Western Star trucks equipped with side air intakes on the hood. The stainless steel cover may loosen and detach, creating a road hazard and increasing crash risk.
CPSC recalls biOrigins sodium hydroxide products sold on Amazon from July 2020 through July 2021 due to non-child-resistant packaging and missing hazard label information. The product poses risk of chemical burns and skin/eye irritation to children.