FDA Device recall Z-1440-2022
Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS) by Becton Dickinson And, citing may have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, unde….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1440-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-05-09 |
| Published | 2022-07-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
Reason
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
Identifiers
| code_info | GTIN: 382903836871 Lot Numbers/Exp.Date: 1082428 3/31/2024 1097856 3/31/2024 1111860 4/30/2024 1188909 6/30/2024 1208182 7/31/2024 1179403 6/30/2024 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1440-2022%22
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