Centurion Medical Products Corporation recalls CAP BUNDLE KIT DYNDC2137
Recalled Product
CAP BUNDLE KIT DYNDC2137
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: 2018091390 2018120590
View official government recall
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