State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Spiraledge is recalling Everyday Yoga backless chairs because they can break at the rear support rod, posing a fall hazard. One minor injury has been reported.
COVIDIEN LLC is recalling Dermacea Gauze Fluff Rolls due to a potential seal defect that could compromise sterility.
Olympus is recalling 3,701 Rhino Laryngo scope ENF-VT2 units because using non-Olympus accessories may loosen the instrument channel port.
Wismettac Asian Foods is recalling Everyburger chocolate cookies because a sticker partially covers the ingredient list and allergen information.
B. Braun Medical is recalling 190 units of Contiplex Echo OT catheter connectors because they may not stay closed, causing leakage or disconnection.
B. Braun Medical is recalling 2,790 CE17TK epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 168 Contiplex Tuohy Ultra 2-in-1 connector sets because the connectors may not stay closed, leading to leakage or disconnection.
Ortho-Clinical Diagnostics is recalling VITROS Sodium Slides due to a potential for positively biased results. The recall covers multiple generations and expiry dates distributed globally.
B. Braun Medical is recalling CE18TBLS epidural tray connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE18TK ACCU-BLOC PERIFIX Kits because the catheter connectors may not stay closed, causing leakage or disconnection.
B. Braun Medical is recalling Perifix One Epidural Full Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
Coviden is recalling 1,902 EEA Circular Staplers with Tri-Staple Technology due to a potential defect that may cause incomplete staple formation or device retention in tissue.
B. Braun Medical is recalling Contiplex Tuohy Ultra catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling specific epidural catheter connectors that may not stay closed, leading to potential leakage or disconnection.
B. Braun Medical is recalling 2,800 clamp style catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE18H Continuous Epidural Sets because the catheter connectors may not stay closed, potentially causing leakage or disconnection.
B. Braun Medical is recalling CE17TKFC Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling ESPOCAN Combined 27GA catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 120 catheter connector kits because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling Contiplex Cont Nerve Block connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 880 units of CNB200TKU Non-Stim Catheter Full Kits because the connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 5,460 units of CNB200T Contiplex Tuohy Sets because the catheter connectors may not stay closed, leading to leakage or disconnection.
COVIDIEN LLC is recalling Kerlix Bandage Rolls due to a potential seal defect that could compromise product sterility.
B. Braun Medical is recalling EC19OF Springwound 19G epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
Olympus is recalling 5,845 Bronchovideoscope BF-Q180 units because using non-Olympus accessories may have caused the instrument channel port to loosen.