Device recall
Z-2264-2020: PerkinElmer 226 Sample Collection Device
FDA device recall · Class III · PerkinElmer Health Sciences, Inc.
Key facts
| Recall number (Z-number) | Z-2264-2020 |
|---|---|
| Recall event | 85630 |
| Product | PerkinElmer 226 Sample Collection Device |
| Product code | PJC |
| Recalling firm | PerkinElmer Health Sciences, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 26, 2021 |
| 510(k) numbers | K121864 |
| FEI number | 3007145015 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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