Device recall
Z-1378-05: SmartCycler Diagnostic Software for use with Cepheid brand SmartCycler Real Time…
FDA device recall · Class II · Cepheid
Key facts
| Recall number (Z-number) | Z-1378-05 |
|---|---|
| Recall event | 32756 |
| Product | SmartCycler Diagnostic Software for use with Cepheid brand SmartCycler Real Time PCR Thermocycler |
| Product code | NSR |
| Recalling firm | Cepheid |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2006 |
| 510(k) numbers | K0022504 |
| FEI number | 3004530258 |
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