Device recall
Z-2121-2012: Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product…
FDA device recall · Class II · Perkinelmer
Key facts
| Recall number (Z-number) | Z-2121-2012 |
|---|---|
| Recall event | 62512 |
| Product | Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product Usage: The GSP instrument is a fully automated, high throughput batch analyzer for time- resolved and prompt fluorescence analysis of samples in microtitration plates. It is intended for in vitro quantitative /… |
| Product code | JLW |
| Recalling firm | Perkinelmer |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 18, 2014 |
| 510(k) numbers | K090846 |
| FEI number | 3006159931 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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