State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Anderson Compounding Pharmacy is recalling Gentamicin 250 mg/1000 mL Irrigation due to a lack of sterility assurance. The recall covers 4 bottles distributed nationwide.
Anderson Compounding Pharmacy is recalling Dexamethasone 24 mg/mL Injection vials due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling 276 vials of a methionine and choline injection nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix Injection nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Serum Tears 20% Drops due to a lack of sterility assurance. All lots of the 1 mL droptainers are affected.
Anderson Compounding Pharmacy is recalling HCG 20,000 units/vial products nationwide due to a lack of sterility assurance.
Porsche is recalling 2010-2016 Panamera vehicles because water in the A/C blower control unit can cause an electrical short and fire.
Anderson Compounding Pharmacy is recalling Gentamicin 160 mg/1000 mL Sterile Water for Irrigation due to a lack of sterility assurance.
MSM Nutraceuticals is recalling Dry Eye Eye Drops because the product was not terminally sterilized and was not tested per USP 71.
Anderson Compounding Pharmacy is recalling HCG 11,000 Units vials nationwide because the product lacks sterility assurance.
Anderson Compounding Pharmacy is recalling 57 vials of HCG 30 Day due to a lack of sterility assurance. The products were distributed nationwide.
ICU Medical is recalling specific lots of ChemoLock devices because they may contain plastic burr particulate from the protective cap.
Anderson Compounding Pharmacy is recalling Prostaglandin 60 mcg/mL vials nationwide due to a lack of sterility assurance.
LDJ is recalling 2017-2018 R250 Container trailers because axles may be installed backwards or unwelded, potentially causing brake failure and increasing crash risk.
ICU Medical is recalling specific lots of ChemoClave Vial Spikes because they may contain plastic burr particulate from the protective cap.
Anderson Compounding Pharmacy is recalling Amphotericin B 0.15% Eye Drops due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling Heparin and Marcaine syringes due to a lack of sterility assurance. The recall covers all lots distributed nationwide.
Anderson Compounding Pharmacy is recalling Vancomycin 125 mg/3mL Inhalation vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling HCG 23 Day Injection Extra Strength vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Papaverine 30 mg/mL Injection vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Polyhexamethylene Biguanide 0.02% Ophthalmic Drops due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Streptomycin 24 mg/Dexamethasone 10 mg/mL Otic Injection due to a lack of sterility assurance.
Gyrus ACMI, Inc. is recalling Diego Elite Turbinate Blades because they may allow unintended RF energy activation when used with Olympus consoles.
Anderson Compounding Pharmacy is recalling Prostaglandin Tri-Mix 20:25:1 Injection vials nationwide due to a lack of sterility assurance.
Anderson Compounding Pharmacy is recalling Morphine Sulfate 5 mg/3mL inhalation vials due to a lack of sterility assurance. The recall covers 60 vials distributed nationwide.