Device recall
Z-1928-2019: cobas p 701 post-analytical units, Part Number 05349966001. For diagnostic…
FDA device recall · Class III · Roche Diagnostics Corporation
Key facts
| Recall number (Z-number) | Z-1928-2019 |
|---|---|
| Recall event | 82651 |
| Product | cobas p 701 post-analytical units, Part Number 05349966001. For diagnostic sample storage and retrieval. |
| Product code | JQP |
| Recalling firm | Roche Diagnostics Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 12, 2020 |
| FEI number | 1823260 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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