The Recall Desk
HighFDA (Devices)·Z-0207-2022·Announced 2021-11-17

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.
Category
Medical Device — Phlebotomy / Blood Collection
Hazard

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.

Part of a larger recall action

This product is one of 6 recalled by Zhejiang Kindly Medical Devices Co., Ltd. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →

Related recalls

Same manufacturer · Zhejiang Kindly Medical Devices Co., Ltd.

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Same hazard · safety mechanism failure

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