FDA Device recall Z-0089-2020
CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
- FDA Device
- Class II
- terminated
- Published 2019-10-16
On 2019-10-16 the FDA classified a Class II recall of CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 by Centurion Medical Products, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0089-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-24 |
| Published | 2019-10-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Centurion Medical Products |
| Distribution | US |
Product
CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
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.
Identifiers
| code_info | 2018012450 2018020850 2018062750 2018071250 2018090650 2018101250 2019022550 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0089-2020%22
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