FDA Device recall Z-0103-2020
IV SECUREMENT KIT IVS3405
- FDA Device
- Class II
- terminated
- Published 2019-10-16
On 2019-10-16 the FDA classified a Class II recall of IV SECUREMENT KIT IVS3405 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-0103-2020 |
| 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
IV SECUREMENT KIT IVS3405
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 | 2019031490 2017100690 2017110790 2018011790 2018050490 2018060590 2018072490 2018110190 2019011490 2019020690 |
|---|
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-0103-2020%22
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