Device recall
Z-0690-2013: Microplate, truncated V-bottomed lots included in the above listed products…
FDA device recall · Class II · Perkinelmer
Key facts
| Recall number (Z-number) | Z-0690-2013 |
|---|---|
| Recall event | 63771 |
| Product | Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS Microplate is a general purpose 96 well microplate used in the preparation and examination of specimens from the human body. |
| Recalling firm | Perkinelmer |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 7, 2014 |
| 510(k) numbers | K071649 |
| FEI number | 3006159931 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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