State
73,741 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Oridion Medical is recalling 192 CapnoStream 20P patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
Olympus is recalling 2,803 Bronchovideoscope BF-1T60 units because using non-Olympus accessories may loosen the instrument channel port.
B. Braun Medical is recalling 590 CONTI ECHO CT catheter connector sets because they may not stay closed, leading to leakage or disconnection.
Oridion Medical is recalling 1,038 CapnoStream 20P bedside patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
B. Braun Medical is recalling 1,030 epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE17TKFCPS Epidural Full Tray connectors because they may not stay closed, leading to leakage or disconnection.
Canyon is recalling about 820 model year 2018 Spectral mountain bikes because the aluminum chainstays can crack, posing a crash hazard.
B. Braun Medical is recalling 2,420 epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
COVIDIEN LLC is recalling Dermacea Gauze Fluff Rolls due to a potential seal defect that could compromise product sterility.
B. Braun Medical is recalling 372 CE18TIN epidural set connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE18HKPS Continuous Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE17TKST epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 108 Contiplex Cont Nerve Block connectors because they may not stay closed, leading to leakage or disconnection.
Oridion Medical is recalling CAPNOSTREAM 20P bedside patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
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.
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.