State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lipari Foods is recalling Premo and Fresh Grab Ham & Cheese wheat sandwiches because they contain chicken recalled for potential Listeria monocytogenes contamination.
Lipari Foods is recalling Premo Signature Cranberry Almond Chicken Salad croissant sandwiches because the chicken may be contaminated with Listeria monocytogenes.
Lipari Foods is recalling Premo and Fresh Grab Chicken Salad wheat sandwiches because the chicken may be contaminated with Listeria monocytogenes.
Northern Tier Bakery LLC is recalling chicken salad sandwiches due to potential Listeria monocytogenes contamination. Products were distributed in Minnesota and Wisconsin.
Avella of Deer Valley, Inc. is recalling 808 droptainers of Povidone Iodine, 5% Ophthalmic Solution due to a lack of sterility assurance.
Altec Industries is recalling 2018-2019 aerial devices that were not stability tested according to ANSI A92.2 standards, posing a risk of collapse.
Coborn's, Inc. is recalling Chicken Salad on Marble Rye sandwiches due to the potential for Listeria monocytogenes contamination.
Coborn's is recalling Chicken Salad Croissant Sandwiches because they may be contaminated with Listeria monocytogenes. The products were distributed in Minnesota, North Dakota, South Dakota, and Wisconsin.
Nephron Pharmaceuticals is recalling 162 bags of Amino Acid Injection due to lack of sterility assurance and potential leaks.
Nephron Pharmaceuticals is recalling 1,047 bags of del Nido Cardioplegia Solution because the bags may leak, compromising sterility.
Nephron Pharmaceuticals is recalling 1,855 bags of Fentanyl Citrate and Bupivacaine HCl injection due to potential glass contamination.
Exactech, Inc. is recalling 158 Ergo 3.2mm K-wires because they may fracture at the threads and remain in the glenoid during shoulder surgery.
Nephron Pharmaceuticals is recalling 1,370 bags of Fentanyl Citrate and Bupivacaine HCl injection due to potential glass contamination.
Nephron Pharmaceuticals is recalling 615 bags of Fentanyl and Ropivacaine Injection due to potential glass contamination from GMP deviations.
GN Otometrics is recalling 3,071 ICS CHARTR EP 200 units because undergrounded electrical surfaces may cause electrical shock to patients or healthcare professionals.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may separate during use in specific legacy devices.
Andover Healthcare Inc. is recalling 1,759 cases of sterile Co-Flex LF2 wound dressings because of incomplete packaging seals, which may compromise sterility.
Candela Corporation is recalling HFC-134a coolant canisters because the neck bushing may become loose and separate from the canister body during use.
Kawasaki is recalling about 1,100 lawn mower engines because a damaged fuel line can leak fuel, posing burn and fire risks.
Community Products is recalling 1,079 Rifton TRAM Low Base powered lift devices because a design change makes the latch springs susceptible to fatigue failure.
GE Healthcare is recalling ApexPro Telemetry Server Systems because they may fail to provide visual or audible alarms for ECG arrhythmias, lead failures, or pulse oximetry issues.
Smiths Medical ASD Inc. is recalling GRIPPER Needles because some may be occluded or blocked, posing a risk to patients.
Temp-Air is recalling 2017-2019 EBB-80 trailers because an incorrect hitch coupling may limit adjustability, potentially causing the trailer to drag and increasing crash risk.
Beckman Coulter is recalling Lipase assays because acetaminophen metabolites cause negative interference in overdose patients.
Community Products, LLC is recalling 3,282 Rifton TRAM Standard Base powered lift devices due to a design defect that may cause the latch mechanism to fail after repeated use.