Device recall
Z-2410-2019: DRG Salivary Progesterone HS ELISA- IVD for the determination of progesterone in…
FDA device recall · Class II · DRG Instruments GmbH
Key facts
| Recall number (Z-number) | Z-2410-2019 |
|---|---|
| Recall event | 83177 |
| Product | DRG Salivary Progesterone HS ELISA- IVD for the determination of progesterone in human saliva REF: SLV-5911 in vitro diagnostic |
| Product code | JLS |
| Recalling firm | DRG Instruments GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2020 |
| FEI number | 3002800697 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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