State
73,598 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, 1,137 (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 7,844 recalls whose distribution notice names Minnesota specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Russ Davis Wholesale Inc. is recalling 536 units of Veggie Pizza sold in six states because the product contains undeclared soy lecithin.
Trek is recalling Bontrager Satellite City bicycle pedals because they may fall off the crank arm, posing fall and injury hazards to riders.
Conagra Brands is recalling Udi Gluten Free Chocolate Zucchini Muffins due to the potential presence of plastic. Consumers should stop eating the product.
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to defects in the distal connector that may prevent proper catheter passage or locking.
Biopsybell is recalling 40 units of 10G coaxial cannulas labeled as sterile but potentially not sterilized. The units were distributed in Mississippi and Kentucky.
RaySearch Laboratories is recalling RayStation and RayPlan software versions due to a defect that may mislabel approximate radiation doses as clinical doses.
PepsiCo is recalling Evolve Vanilla Bean Plant-Based Protein Shakes because they contain undeclared soy. The recall covers 14,830 cases distributed nationwide.
Conagra Brands is recalling Udi Gluten Free Double Chocolate Muffins due to the potential presence of plastic.
Bard Access Systems is recalling specific Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Fresenius Medical Care is recalling 709 cases of Delflex Peritoneal Dialysis Solution because a 4.25% dextrose bag was found inside a 1.5% dextrose box.
Bard Access Systems is recalling specific Groshong NXT ClearVue catheters due to defects in the distal connector that may prevent proper catheter passage or locking.
W.L. Gore & Associates is recalling 61 Gore Viabil Biliary Endoprosthesis devices because a complaint reported a device appeared shorter than its labeled length.
Sun Pharmaceutical Industries is recalling CEQUA (cyclosporine) ophthalmic solution due to subpotent drug levels and the presence of particulates.
Boston Scientific is recalling 27 units of the ELUVIA Drug-Eluting Vascular Stent System because some 6x40mm stents were incorrectly placed in 6x100mm packaging.
NOW Health Group is recalling 10,235 bottles of NOW 4x6 Acidophilus because foreign capsules were found in the product.
Conagra Brands is recalling Udi Gluten Free Blueberry Muffins due to the potential presence of plastic. Consumers should check lot codes and stop eating the product.
KVK-Tech, Inc. is recalling 17,096 bottles of Hydrocodone Bitartrate and Homatropine Methylibromide tablets due to failed impurities and degradation specifications.
SigmaPharm Laboratories is recalling Asenapine sublingual tablets because they were manufactured with the wrong flavoring agent.
Nomax Inc. is voluntarily recalling 78 cartons of Dry Eye Test strips due to subpotent drug content. The FDA classified this as a Class III recall.
SigmaPharm Laboratories LLC is recalling Asenapine Sublingual Tablets because they were manufactured with the incorrect flavoring agent.
Tesla is recalling 2019-2021 Model Y vehicles because seat belt retractor fasteners may not be properly attached, increasing injury risk.
Van Hool is recalling 681 buses because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.
Life Line Emergency Vehicles is recalling 2019-2020 RAM 5500 vehicles because improperly routed rear brake lines may chafe and leak fluid, increasing crash risk.
Tesla is recalling 2018-2020 Model 3 and 2019-2021 Model Y vehicles because front seat belt fasteners may not be properly attached, increasing injury risk.
Tesla is recalling certain 2020 Model 3 vehicles because brake caliper bolts may loosen, causing the caliper to separate and lose tire pressure, increasing crash risk.