State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fresh Express is recalling Green & Crisp salad products containing iceberg lettuce, red cabbage, and carrots due to a possible health risk from Cyclospora.
Skeletal Kinetics is recalling 60 units of Ossilix MP Fil bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.
Skeletal Kinetics is recalling Osteovation bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Fresh Express is recalling Marketside Baby Greens Salad due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.
Fresh Express is recalling Marketside Tri-Color Cole Slaw due to a possible health risk from Cyclospora. The product is sold in specific US states and Canada.
Skeletal Kinetics is recalling SKAFFOLD CMF Impress bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Fresh Express is recalling Fancy Greens salad products due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.
Fresh Express Incorporated is recalling Chopped Kit Poppyseed salads due to a possible health risk from Cyclospora.
Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing incomplete bone formation.
Fresh Express is recalling Hy-Vee Chopped Kit Avocado Ranch Salad products due to a possible health risk from Cyclospora.
Garland Ventures is recalling Freshness Guaranteed Five Cheese Stuffed Shells due to potential Listeria monocytogenes contamination.
Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Fresh Express is recalling 14 oz 3 Color Deli Cole Slaw due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.
Skeletal Kinetics is recalling Craniosculpt bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Fresh Express is recalling Hy-Vee Chopped Kit Southwest Salad due to a possible health risk from Cyclospora. Consumers should not eat the product.
Fresh Express is recalling Giant Eagle Chopped BBQ Ranch Salad Kits due to a possible health risk from Cyclospora contamination.
Fresh Express is recalling Marketside Chopped Salad Kits due to a possible health risk from Cyclospora. Consumers should not consume the affected products.
Akorn, Inc. is recalling Proparacaine Hydrochloride Ophthalmic Solution, 0.5%, due to chemical contamination from equipment cleaning residue.
Preferred Pharmaceuticals is recalling Lidothol Patches because the contract manufacturer misplaced or lost batch records and test results.
Shimadzu Medical Systems is recalling three Trinias DAP Meters because they were found to be outside of tolerance. The devices are used in interventional procedures.
DJO, LLC is recalling Nylatex wraps used with Intelect and V-Sonic devices because they lack appropriate latex warning labels.
Keryx Biopharmaceuticals is recalling 59,820 bottles of Auryxia (ferric citrate) tablets because they were not manufactured in conformance with the FDA-approved process.
RemedyRepack Inc. is recalling Carbamazepine 200 mg tablets because routine stability testing revealed low dissolution results.
Neocis Inc. is recalling 70 units of Gen 2 Posterior Chairside Splints due to potential mislabeling. The affected products are used in dental implantation surgery.
Neocis Inc. is recalling specific dental chairside splints because they may be mislabeled. The recall covers 70 units distributed nationwide.