Device recall
Z-1140-03: Anti-dsDNA [125I] Radiobinding Assay Kit. For In-Vitro Diagnostic Use Catalog…
FDA device recall · Class III · Perkinelmer Life Sciences, Inc.
Key facts
| Recall number (Z-number) | Z-1140-03 |
|---|---|
| Recall event | 26856 |
| Product | Anti-dsDNA [125I] Radiobinding Assay Kit. For In-Vitro Diagnostic Use Catalog Number: NEA 103 |
| Product code | DHN |
| Recalling firm | Perkinelmer Life Sciences, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 19, 2003 |
| 510(k) numbers | K843347 |
| FEI number | 1000513616 |
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