FDA Device recall Z-1439-2022
BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (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-1439-2022 |
| 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
BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (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: N/A Lot Numbers/Exp.Date: 1127328 |
|---|
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-1439-2022%22
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