Device recall
Z-2756-2017: PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection…
FDA device recall · Class III · PerkinElmer Health Sciences, Inc.
Key facts
| Recall number (Z-number) | Z-2756-2017 |
|---|---|
| Recall event | 77668 |
| Product | PerkinElmer 226 Sample Collection Device The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory in Newborn Screening. |
| Product code | PJC |
| Recalling firm | PerkinElmer Health Sciences, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2017 |
| 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