State
73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Steris is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low, potentially causing false results in steam sterilization monitoring.
Apothecary Pharma LLC is recalling 22 vials of Tirzepatide Injection due to a lack of assurance of sterility. The affected product was distributed nationwide.
K.C. Pharmaceuticals is recalling Good Sense Eye Drops Irritation Relief and related brands due to a lack of assurance of sterility.
K.C. Pharmaceuticals is recalling multiple brands of eye drops, including Leader, Equate, and Walgreens, due to a lack of assurance of sterility.
Medline is recalling 1,824 bariatric rollators because the front wheel assembly may detach, posing a risk of falls and serious injury.
KTM is recalling certain Müller Präzision steering dampers for 2020-2026 KTM Super Duke R and Evo motorcycles because they can loosen, leading to loss of steering control.
Medtronic is recalling 20 MiniMed Flex insulin pumps that failed or lacked verification test results, posing risks of inaccurate insulin delivery and device malfunctions.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
A&P CREATIONS is recalling X10 Natural Enhancement Supplement because it contains undeclared Sildenafil and Tadalafil.
K.C. Pharmaceuticals is recalling 505,896 cartons of artificial tears sold under multiple brands because the product lacks assurance of sterility.
Carolina Infusion, LLC is recalling Sermorelin Acetate 1 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Carolina Infusion, LLC is recalling specific lots of Tirzepatide/Cyanocobalamin 64/2 mg/mL injectable because the product may lack assurance of sterility.
Carolina Infusion, LLC is recalling Semaglutide 3 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Carolina Infusion, LLC is recalling Tirzepatide 26 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Steris Corporation is recalling 217 VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false sterilization results.
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used in compounding raised concerns about the product's sterility.
K.C. Pharmaceuticals is recalling Good Sense Eye Drops Original Formula due to a lack of assurance of sterility. The recall affects 1,025,448 cartons distributed nationwide.
Safeguard US Operating LLC is recalling 46,881 units of compression bandages and trauma kits because the bandages may be degraded, posing a risk of introducing foreign material into wounds.
Medline is recalling 835 bariatric rollators because the front wheel assembly may disconnect from the frame, posing a risk of falls and severe injuries.
Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification.
Intellijoint Surgical is recalling eight navigation systems because their workstations may contain a defective Apple battery that could overheat and cause a fire.
Steris Corporation is recalling VERIFY Biological Steam Test Packs because the spore population may fall below specifications, potentially causing false-negative steam sterilization results.
Carolina Infusion, LLC is recalling Tri-MIX compounded syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Steris is recalling VERIFY Dual Species Self-Contained Biological Indicators because spore populations may fall below specifications, potentially leading to false sterilization results.