Device recall
Z-0030-2014: Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900…
FDA device recall · Class II · Perkin Elmer Health Sciences, Inc.
Key facts
| Recall number (Z-number) | Z-0030-2014 |
|---|---|
| Recall event | 66310 |
| Product | Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the… |
| Product code | JKA |
| Recalling firm | Perkin Elmer Health Sciences, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2014 |
| 510(k) numbers | K121864 |
| FEI number | 3007145015 |
At a glance
- 1–9 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