Device recall
Z-0209-2022: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068…
FDA device recall · Class II · Zhejiang Kindly Medical Devices Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0209-2022 |
|---|---|
| Recall event | 88757 |
| Product | HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm |
| Product code | FMI |
| Recalling firm | Zhejiang Kindly Medical Devices Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 21, 2023 |
| FEI number | 3003560965 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database