Class II — Zhejiang Kindly Medical Devices Co., Ltd.
| Recalling firm | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
|---|---|
| Registered facility | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for difficulty in safety mechanism activation. |
| Product | HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm |
| Quantity | N/A |
| Distribution | U.S. Nationwide distribution. |
| Initiated | 2021-08-24 |
| Classified | 2021-11-05 |
| Terminated | 2023-07-21 |
| Recall number | Z-0209-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Zhejiang Kindly Medical Devices Co., Ltd. (Z-0209-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88757/
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