FDA Device recall Z-0205-2022
McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
- FDA Device
- Class II
- terminated
- Published 2021-11-17
On 2021-11-17 the FDA classified a Class II recall of McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS by Zhejiang Kindly Medical Devices, citing potential for difficulty in safety mechanism activation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0205-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-08-24 |
| Published | 2021-11-17 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Zhejiang Kindly Medical Devices |
| Distribution | US |
Product
McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
Reason
Potential for difficulty in safety mechanism activation.
Identifiers
| code_info | Lot numbers / Expiration Date: CKDI11-01 / Exp. Date 2024-10-01, CKDI11-02 / Exp. Date 2024-10-02, CKDI12-01 / Exp. D…Lot numbers / Expiration Date: CKDI11-01 / Exp. Date 2024-10-01, CKDI11-02 / Exp. Date 2024-10-02, CKDI12-01 / Exp. Date 2024-11-01, CKDJ01-01 / Exp. Date 2024-12-01, CKDJ03-01 / Exp. Date 2025-02-01, CKDJ05-01 / Exp. Date 2025-04-01, CKDJ05-03 / Exp. Date 2025-04-03, CKDJ06-01 / Exp. Date 2025-05-01, CKDJ12-01 / Exp. Date 2025-11-01. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0205-2022%22
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