HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch — Class II medical device recall Z-0208-2022
Terminated recall by Zhejiang Kindly Medical Devices Co., Ltd., reported 2021-11-17, distributed nationwide. Potential for difficulty in safety mechanism activation.
| Recall number | Z-0208-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zhejiang Kindly Medical Devices Co., Ltd., Wenzhou, N/A, China |
| Recall initiated | 2021-08-24 |
| Classified | 2021-11-05 |
| Reported by FDA | 2021-11-17 |
| Terminated | 2023-07-21 |
| Distributed | Nationwide (US) |
| Lot numbers | 20201030, 20201210, 2025.10.29, 2025.12.09 |
| Model numbers | 1000PCS/CTN, 100PCS/BOX, 570-2067 |
Product
HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch, REF 570-2067, 100pcs/box 1000pcs/ctn 350*210*350mm
Reason for recall
Potential for difficulty in safety mechanism activation.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0208-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.