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Recall Observatory FDA recall evidence

Device product

TRIPLE LUMEN BUNDLE KIT ECVC1540

Z-0088-2020

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-0088-2020

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: 2017102650 2018010550 2018020850 2018042650 2018071650 2018081050 2018090450 2018100950 2018101750 2019032250

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.