McKesson PREVENT HT Winged Blood Collection Needles Recall for Safety Mechanism Difficulty
McKesson PREVENT HT Safety Winged Blood Collection Needles may have difficulty activating their safety mechanism. The recall affects units distributed nationwide.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II medical device recall for a potential safety mechanism failure on a blood collection needle. No injuries or deaths have been reported; the hazard is theoretical. Per the rubric, this qualifies as High (score 3) for a risk-of-harm product where injury has not yet been reported.
Plain-English summary
McKesson PREVENT HT Safety Winged Blood Collection Needles with Tube Holder (MFR # 16-NBCH21GS), manufactured by Zhejiang Kindly Medical Devices Co., Ltd., are being recalled by the FDA. The devices may have difficulty activating their safety mechanism.
The affected products were distributed nationwide in the United States. Seven lot numbers are included in the recall: CKDI11-01 through CKDJ06-01, with expiration dates from October 2024 to May 2025.
This FDA Class II recall was issued as Z-0207-2022.
The recalled product
- Product
- McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH21GS
- Manufacturer
- Zhejiang Kindly Medical Devices Co., Ltd.
- Hazard
- safety-mechanism-failure
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (7)
- Lot Numbers / Expiration Dates: 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
- CKDJ05-03 / Exp. Date 2025-04-03
- CKDJ06-01 / Exp. Date 2025-05-01.
Distribution
Distributed nationwide across the United States.
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