State
73,817 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,851 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 2,246 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Advanced Pharma Inc. is recalling all Lidocaine products because they may contain latex but lack appropriate labeling.
Advanced Pharma Inc. is recalling Ofirmev (Acetaminophen) injection because the product may contain synthetic or natural latex, which is not currently classified in the labeling.
Teleflex Medical is recalling 19,043 units of PE Connector 3/8 Straight 20/BX because the expiration date is missing from the labeling, creating a risk that expired product may be used.
Advanced Pharma Inc. is recalling TPN products because they may contain latex but lack proper labeling.
Teleflex Medical is recalling 19,043 units of PE Connector 3/8 Y 20/BX because the expiration date is missing from the labeling, creating a risk of using expired product.
Advanced Pharma Inc. is recalling all lots of Norepinephrine Bitartrate because the product may contain synthetic or natural latex, which is not currently disclosed on the label.
Advanced Pharma Inc. is recalling Ropivacaine HCl in 0.9% Sodium Chloride because the product may contain synthetic or natural latex, which is not currently classified in the labeling.
Advanced Pharma Inc. is recalling all lots of Nalbuphine because the product labeling fails to disclose that it may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Lorazepam HCl because the product may contain synthetic or natural latex, which is not currently labeled.
Advanced Pharma Inc. is recalling Fentanyl Citrate and Bupivacaine HCl products because labeling may not disclose the presence of synthetic or natural latex.
Advanced Pharma Inc. is recalling NICU Starter TPN products because they may contain synthetic or natural latex without proper labeling.
Advanced Pharma Inc. is recalling all lots of Vancomycin HCl because the product may contain latex but lacks appropriate labeling.
Advanced Pharma Inc. is recalling all lots of Fentanyl Citrate because the product labeling does not indicate that it may contain synthetic or natural latex.
Advanced Pharma Inc. is recalling all lots of Meperidine HCl because the product labeling does not indicate that it may contain synthetic or natural latex.
Mesa Laboratories is recalling 9,900 units of Conductivity/TDS Calibrator Solution because the product failed to meet specifications. The solution is used for calibrating hemodialysis equipment and does not contact patients.
Advanced Pharma Inc. is recalling 0.9% Sodium Chloride Slip Tip products because they may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Heparin sodium because the product may contain synthetic or natural latex without proper labeling.
Advanced Pharma Inc. is recalling Sodium Phosphate products because they may contain latex but lack proper labeling. The recall covers all strengths and dosage forms distributed nationwide.
BioMerieux SA is recalling Ceftriaxone ETEST kits due to a potential performance issue affecting strain categorization.
Advanced Pharma Inc. is recalling Calcium Gluconate products because they may contain latex without proper labeling.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Sodium Citrate because the product may contain latex without proper labeling.
Siemens Medical Solutions is recalling 4,095 AXIOM Sensis diagnostic computers because dust accumulation can cause system failures, potentially interrupting clinical treatments.
Advanced Pharma Inc. is recalling all strengths and dosage forms of Potassium Phosphate because the product may contain latex but lacks proper labeling.
Advanced Pharma Inc. is recalling Cardioplegic Solution Maintenance due to a labeling error regarding potential latex content.
Advanced Pharma Inc. is recalling all lots of Midazolam HCl because the product may contain synthetic or natural latex.