Device recall
Z-1436-2011: Gen-Probe AccuProbe Group B Streptococcus Culture Identification Test Kit, 2820.
FDA device recall · Class I · Gen-Probe Inc
Key facts
| Recall number (Z-number) | Z-1436-2011 |
|---|---|
| Recall event | 55432 |
| Product | Gen-Probe AccuProbe Group B Streptococcus Culture Identification Test Kit, 2820. |
| Product code | MDK |
| Recalling firm | Gen-Probe Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 8, 2011 |
| 510(k) numbers | K974572 |
| FEI number | 2024800 |
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