Z-0206-2022 Class II Terminated
FDA device recall Z-0206-2022 was initiated by Zhejiang Kindly Medical Devices Co., Ltd. on August 24, 2021 and is designated Class II. Reason for recall: Potential for difficulty in safety mechanism activation. The recall status is terminated (terminated July 21, 2023). Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- November 17, 2021
- Initiation Date
- August 24, 2021
- Termination Date
- July 21, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH22GS
Reason for Recall
Potential for difficulty in safety mechanism activation.
Distribution Pattern
U.S. Nationwide distribution.
Code Information
Lot Numbers / Expiration Date: CKDI11-01 / Exp. Date 2024-10-01, 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.