PlainRecalls
FDA Devices Moderate Class II Terminated

STERILE CAP CHANGE KIT DYNDC1946B

Reported: October 16, 2019 Initiated: April 24, 2019 #Z-0086-2020

Product Description

STERILE CAP CHANGE KIT DYNDC1946B

Reason for Recall

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.

Details

Units Affected
181965 total
Distribution
Nationwide domestic distribution.
Location
Williamston, MI

Frequently Asked Questions

What product was recalled?
STERILE CAP CHANGE KIT DYNDC1946B. Recalled by Centurion Medical Products Corporation. Units affected: 181965 total.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 16, 2019. Severity: Moderate. Recall number: Z-0086-2020.