State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Polymer Technology Systems is recalling specific CHOL+HDL+GLU test strips because they show under-recovery when tested against a reference method.
Ortho Clinical Diagnostics is recalling Urine Electrolyte Diluent because the product may become unstable when stored in a 2mL cup for 7 days.
Cardinal Health is correcting labeling on Cordis Precise Nitinol Stent Systems because the instructions incorrectly stated the device was MRI Safe instead of MRI Conditional.
Spectrum Laboratory Products is recalling specific lots of Estriol Micronized USP because assay results did not meet specifications.
Cardinal Health is correcting labeling on S.M.A.R.T. stents that incorrectly stated they were MRI Safe. The correct classification is MRI Conditional.
Lifelines Neuro is recalling 12 ElectroTek Temporal Sensor Cables due to potential incorrect placement labels that could lead to improper electrode placement during EEG studies.
Lifelines Neuro is recalling eight ElectroTek EEG temporal sensor cables because incorrect placement labels could lead to improper electrode positioning during brain activity studies.
Abbott Medical is recalling 470 radiofrequency cannulas that were incorrectly labeled with a 5mm active tip length instead of 10mm.
Ortho Clinical Diagnostics is recalling VITROS 7% BSA diluent because it may become unstable when stored in a 2mL cup for seven days.
Diagnostica Stago is recalling 5,437 units of STA System Control N + P because a positive bias was confirmed on specific calibrator levels.
Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential under-recovery of sample results.
Pharmedium Services LLC is voluntarily recalling 864 bags of repinephrine bitartrate injection because the drug was subpotent. The recall covers nationwide distribution in the U.S.
Tosoh Smd Inc is recalling AIA-PACK B12 Pretreatment Sets due to barcode scanning issues that may delay diagnostic results.
Pharmedium Services LLC is recalling 5,808 bags of Repinephrine Bitartrate Injection due to subpotent drug levels. The FDA classified this as a Class III recall.
Pharmedium Services LLC is voluntarily recalling 5,820 bags of subpotent repinephrine bitartrate injection. The FDA classified this as a Class III recall.
J&J Distributing is recalling approximately 136 pounds of ready-to-eat salad products containing meat because they contain undeclared pine nuts, a tree nut allergen.
Toyne Inc. is recalling 2018-2019 Spartan Metro Star and Gladiator chassis due to a brake relay valve defect that may increase stopping distance.
Autocar is recalling 2015-2020 Xspotter vehicles because the headlamp relay may disconnect, causing headlights to shut off and increasing crash risk.
Motor Coach Industries is recalling 2018-2020 D4500 and D4505 coaches because tag axle clamps may slip, causing misalignment and increasing crash risk.
Autocar is recalling 2016-2019 Xspotter vehicles because the shift pad may fail to display the transmission range, increasing the risk of a crash or injury.
Whole Foods Market is recalling Stir Fry Beef Vegan served on the hot bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Vegetable Power Blend served on the salad bar due to possible contamination with Listeria monocytogenes.
Whole Foods Market is recalling Korean Chicken Bowls due to possible Listeria monocytogenes contamination. The products were sold nationwide from October 10 to November 4, 2019.
Whole Foods Market is recalling Shaved Brussels Sprout Grilled Chicken Bowls due to possible Listeria monocytogenes contamination.
Whole Foods Market is recalling salad bar slaw containing Brussels sprouts, apples, and cheddar due to possible Listeria monocytogenes contamination.