Lower risk Medical device recall · FDA · Published August 24, 2021

Henry Schein Blood Collection Needles: Safety Mechanism Activation Difficulty

Henry Schein recalls 21Gx 1 1/4 inch blood collection needles (REF 570-2067) due to potential safety mechanism activation issues. Affected items have specific lot numbers and expiration dates.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0208-2022Medical device Henry Schein ›

Lower-risk recall

Potential for difficulty in safety mechanism activation.

Take action

Contact the company

Recalling firmZhejiang Kindly Medical Devices Co., Ltd.# 758 Binghai Five Rd., Longwan Dist · Wenzhou, China

✎ GovInfoNow plain-language explainer

Henry Schein is recalling 21Gx 1 1/4 inch blood collection needles with a specific reference number because they may have difficulty activating the safety mechanism. This could lead to improper needle use during blood collection procedures. Read more at govinfonow.com/recall/61905-henry-schein-blood-collection-needles-safety-mechanism-activation-difficulty.

Source Summary by GovInfoNow · govinfonow.com/recall/61905-henry-schein-blood-collection-needles-safety-mechanism-activation-difficulty · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0208-2022

Cite this page

“Henry Schein Blood Collection Needles: Safety Mechanism Activation Difficulty.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61905-henry-schein-blood-collection-needles-safety-mechanism-activation-difficulty. Based on FDA recall #Z-0208-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0208-2022%22&limit=1).

Zhejiang Kindly Medical Devices Co., Ltd. recalled HENRY SCHEIN Safety Blood Collection Needles on Aug. 24, 2021, due to potential difficulty activating the safety mechanism, according to the FDA. The recall involves specific lot numbers distributed nationwide.

How to tell if you have it

Brand: Henry Schein
Product: HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch
REF: 570-2067
Lot Numbers: 20201030, 20201210
Expiration Dates: 2025.10.29, 2025.12.09

The hazard

The needles pose a potential for difficulty in safety mechanism activation, according to the FDA.

Context

GovInfoNow's records show other recent recalls of similar products include B. Braun 21GA Winged Infusion Needle Recall (2026-02-02) and Medline Perfusion Syringe Recall (2025-10-27).

How to tell if you have this one

Check for the product reference number 570-2067 on the packaging. Affected items have lot numbers 20201030 (expires 2025.10.29) or 20201210 (expires 2025.12.09).

Brand
Henry Schein
Category
Medical device

FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Terminated
Distribution
U.S. Nationwide distribution.

Recall number	Product, codes & lots
Z-0204-2022	McKesson PREVENT HT Safety Blood Collection Needles, 21G 1 1/4 inch, MFR # 16-NBC21GS; lot numbers / Expiration Date: CDI11-01 / Exp. Date 2024-10-01, CDKI11-02 / Exp. Date 2024-10-02, CKI12-01 / Exp. Date 2024-11-01, CKDJ01-01 / Exp. Date 2024-12-01, CKDJ05-01 / Exp. Date 2025-04-01, CKDJ06-01 / Ex. Date 2025-05-01.
Z-0205-2022	McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS; 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.
Z-0206-2022	McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH22GS; 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.
Z-0207-2022	McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH21GS; 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.
Z-0208-2022	HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch, REF 570-2067, 100pcs/box 1000pcs/ctn 350210350mm; Lot Numbers / Expiration Date: 20201030 / Exp. Date 2025.10.29, 20201210 / Exp. Date 2025.12.09.
Z-0209-2022	HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350210350mm; Lot Numbers / Expiration Date: 20201030 / Exp. Date 2025.10.29, 20201210 / Exp. Date 2025.12.09.

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the reference number 570-2067 and lot numbers 20201030 or 20201210 on the packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “U.S. Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 23 months after the firm started it.

Aug 24, 2021Firm started the recall
Nov 5, 2021FDA classified it Class II
Nov 17, 2021Published in FDA’s Enforcement Report
Jul 21, 2023FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/61905-henry-schein-blood-collection-needles-safety-mechanism-activation-difficulty">Henry Schein Blood Collection Needles: Safety Mechanism Activation Difficulty (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0208-2022 (August 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0208-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.