Centurion Medical Products Corporation recalls INVASIVE PROCEDURE TRAY MNS9510
Recalled Product
INVASIVE PROCEDURE TRAY MNS9510
Hazard / Issue
Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: 2017100990 2017120490
View official government recall
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