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Recall Observatory FDA recall evidence

Device product

IV SECUREMENT KIT IVS3405

Z-0103-2020

April 24, 2019

Class II

Product summary

Firm
Centurion Medical Products Corporation
Event
Event 83584
Status
Terminated
Classification
Class II
Quantity
181965 total
Official record key
device-enforcement:Z-0103-2020

Official wording

Reason: 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.

Code information: 2019031490 2017100690 2017110790 2018011790 2018050490 2018060590 2018072490 2018110190 2019011490 2019020690

Distribution pattern: Nationwide domestic distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.