CLASS II Device recall · Reported 17 Nov 2021 · FDA Enforcement Report

McKesson Prevent HT Safety Blood Collection Needles recalled

Zhejiang Kindly Medical Devices is recalling McKesson Prevent HT Safety Blood Collection Needles 1, MFR # 16-NBC22GS, distributed nationwide in the US. The recall was initiated on 24 Aug 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 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.
Quantity recalledN/A

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-0205-2022
FDA event ID
88757
Recalling firm
Zhejiang Kindly Medical Devices, Wenzhou, N/A
Classification
Class II
Status
Terminated
Recall initiated
24 Aug 2021
FDA classified
5 Nov 2021
Reported
17 Nov 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

24 Aug 2021Recall initiated by company
5 Nov 2021Classified by FDA+73 days
17 Nov 2021Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for difficulty in safety mechanism activation.

Product as listed by the FDA

McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS

Where it was distributed

U.S. Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

Potential for difficulty in safety mechanism activation.

Which lots are affected?

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.

Where was it sold?

U.S. Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

5 other products · FDA event 88757

This product is part of a recall event; the main page for the event is Henry Schein Safety Blood Collection Needle 21Gx recalled.

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