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.
Kadesh International is recalling Puriton Eye Relief Drops because they were manufactured under non-sterile production conditions.
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Great Dane Trailers is recalling 2019 Freedom Combo Drop Deck Platform trailers because the rear impact guards may be too narrow, potentially failing to prevent vehicles from going under the trailer in a crash.
Virtual Imaging is recalling 253 RadPRO Mobile 40kW Digital X-Ray Systems because the tube head may separate and fall off the unit.
Stryker is recalling 20,030 Spirit Plus hospital beds with high rail siderails due to non-compliance with safety standards and a potential risk of patient entrapment.
R82 A/S is recalling 687 Heron toilet and bath chairs because they contain aluminum gas spring heads. The recall is a replacement campaign for these specific units.
Sandoz Inc. is recalling 18,832 bottles of Isosorbide Dinitrate 20 mg tablets due to cross-contamination with other products.
The Wornick Company is recalling Chef Sensations Fire Roasted diced onion/pepper blend due to potential Salmonella and Listeria contamination.
Arthrex, Inc. is recalling 832 units of the 3.2mm Proximal Reamer/Cannulated Drill because the instrument may break during use.
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Luminex Corporation is recalling 12,700 trays of Verigene Blood Culture Gram-Positive Nucleic Acid Kits due to a potential for false negative results.
Tosoh Bioscience is recalling 393 AIA-900 Analyzers because a pickup arm malfunction can stop the device from testing patient samples, causing delays in results.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Simply Fresh Foods is recalling Rojo's Autentico Black Bean 5 Layer Dip due to potential Salmonella or Listeria monocytogenes contamination in the corn.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
GE Healthcare is recalling Aisys anesthesia systems because a software upgrade prevents the device from automatically switching to backup ventilation if a patient stops breathing.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Medtronic is voluntarily removing Parietex Composite Parastomal Mesh from the market after receiving reports of product failure leading to hernia recurrence.
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
GE Healthcare is recalling Aisys anesthesia systems because they may fail to transition to backup ventilation if a patient stops breathing spontaneously.
Stryker is recalling Spirit Select Beds with high rail siderails due to non-compliance with safety standards and a potential risk of entrapment.
bioMérieux is recalling NucliSENS easyMAG Lysis Buffer because some eluates become colored due to remaining hemoglobin.
Siemens is recalling 14 Artis zee biplane systems because C-arm vibrations may reduce image quality due to a ceiling support screw connection.
Taro Pharmaceuticals is recalling specific bottles of children's allergy relief oral solution because an unknown impurity exceeded safety limits during routine testing.