State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Centurion Medical Products is recalling 600 sterile glass medicine cups because incomplete seals may compromise sterility.
Intuitive Surgical is recalling 123 da Vinci Xi surgical systems worldwide due to potentially defective capacitors that may cause vision loss or system errors.
Cook Inc. is recalling 3,929 PTFE Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Centurion Medical Products Corporation is recalling various suture and laceration trays because incomplete seals on the sterile packages may compromise sterility.
Centurion Medical Products is recalling specific sterile dressing change kits because incomplete seals may compromise sterility. The recall covers kits distributed nationwide and in Ghana.
B. Braun Medical is recalling 5,616 Y-Type Blood Sets because of a potential for leakage at the joint between the blood filters and tubing.
Cook Inc. is recalling 13,388 Urethral Dilation Balloon Catheters because the wire guide may be incorrectly loaded, potentially introducing a stiff tip into the patient.
Centurion Medical Products is recalling Suture Trays because incomplete seals on the sterile package may compromise sterility.
Centurion Medical Products Corporation is recalling various LVAD maintenance kits because incomplete seals on the sterile packages may compromise sterility.
Centurion Medical Products Corporation is recalling 420 PT225 Pain Management Trays due to incomplete seals that may compromise sterility.
Cardinal Health is recalling surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Centurion Medical Products Corporation is recalling specific sterile pitcher kits because incomplete seals may compromise sterility. The products were distributed nationwide and in Ghana.
Centurion Medical Products Corporation is recalling various sterile dressing change trays and procedure kits because incomplete seals may compromise sterility.
Tornel is recalling specific A/T-09 tires due to improper manufacturing that may cause sidewall separation, increasing the risk of tire failure and a crash.
Centurion Medical Products is recalling specific biopsy trays because incomplete sterile package seals may compromise sterility.
Roche Diabetes Care is recalling Accu-Chek Aviva test strips because they may fail to dose, potentially delaying blood glucose results and treatment decisions.
Centurion Medical Products Corporation is recalling HT5555A Hyperalimentation & Dressing Change Trays due to incomplete seals that may compromise sterility.
Centurion Medical Products is recalling various sterile surgical trays and packs because incomplete seals may compromise sterility.
Centurion Medical Products is recalling specific Circumcision Tray Kits because incomplete seals on the sterile packaging may compromise sterility.
Centurion Medical Products Corporation is recalling specific dressing trays and medical packs because incomplete seals may compromise sterility.
Centurion Medical Products is recalling specific sterile biopsy and arthrogram trays due to incomplete seals that may compromise sterility.
Ethicon is recalling specific VICRYL sutures because braid fraying may reduce tensile strength. The recall covers 23,688 units distributed in the US and Puerto Rico.
Cardinal Health is recalling AAMI 3 Nonreinforced Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Cook Inc. is recalling 15 units of Fixed Core Straight Safety Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients.
Cook Inc. is recalling Percutaneous Pigtail Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.