State
73,737 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.
Which agencies issued them
These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
Coviden LLC is recalling Kerlix AMD Antimicrobial Bandage Rolls due to a potential seal defect that could compromise product sterility.
Olympus is recalling 5,607 Bronchofiberscope BF-P40 units because attaching non-Olympus accessories may loosen the instrument channel port.
B. Braun Medical is recalling CE18HKST epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
Cincinnati Sub-Zero is recalling 270 Hemotherm 400CE devices due to potential control panel switch errors that may prevent setting changes or cause unintended changes.
Olympus is recalling 1,874 Bronchovideoscope BF-P160 units because using non-Olympus accessories may loosen the instrument channel port.
B. Braun Medical is recalling CE18TKCD epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE18TKST epidural catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling specific catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE17TKFS Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
Oridion Medical is recalling 264 CAPNOSTREAM 20P bedside patient monitors because date, time, and alarm settings may reset to factory defaults when powered off.
B. Braun Medical is recalling Accu-Bloc Perifix Kits because catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling Perifix Continuous Epidural Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling 60,000 nonsterile Perifix catheter connectors because they may not stay closed, causing leakage or disconnection.
Olympus is recalling 5,810 Bronchovideoscope BF-1T180 units because non-Olympus accessories may cause the instrument channel port to loosen.
B. Braun Medical is recalling EC20O catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling EC20CS Epidural Catheter connectors because they may not stay closed, leading to leakage or disconnection.
Olympus is recalling 3,317 Bronchofiberscope F-1T160 units because using non-Olympus accessories may loosen the instrument channel port.
B. Braun Medical is recalling CE17TBFC Epidural Basic Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling Perifix FX catheter connectors because they may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE17TKFSA full trays because the catheter connectors may not stay closed, leading to leakage or disconnection.
B. Braun Medical is recalling CE18T Continuous Epidural Sets because the catheter connectors 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.