Device recall
Z-2430-2008: Kallestad (TM) Mouse Kidney. Product labeled "BIO-RAD Kallestad (TM) Mouse…
FDA device recall · Class III · Bio-Rad Laboratories
Key facts
| Recall number (Z-number) | Z-2430-2008 |
|---|---|
| Recall event | 49083 |
| Product | Kallestad (TM) Mouse Kidney. Product labeled "BIO-RAD Kallestad (TM) Mouse Kidney Substrate... UNITED STATES, Bio-Rad Laboratories, Redmond, WA 98052... FRANCE, Bio-Rad Laboratories, 92430 Marnes La Coquette". Catalog numbers: 30445 - 8 wells, 48 tests and 30447 - 8 well, 192 tests. |
| Product code | DBL |
| Recalling firm | Bio-Rad Laboratories |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 31, 2011 |
| 510(k) numbers | K792610 |
| FEI number | 3008272466 |
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