FDA Device recall Z-1438-2022
BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (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-1438-2022 |
| 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 White 360 Shelf 100Ea Catalog No. 395000 (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: 382903950003 Lot Numbers/Exp.Date: 1120604 3/31/2024 1098929 3/31/2024 1123643 4/30/2024 1063423 2/29/2024 |
|---|
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-1438-2022%22
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