Device recall
Z-2962-2018: Overhead Counterpoise Systems (OCS), OCS, 580mm CEILING MOUNT, PORTEGRA2…
FDA device recall · Class II · Bayer Medical Care, Inc.
Key facts
| Recall number (Z-number) | Z-2962-2018 |
|---|---|
| Recall event | 80727 |
| Product | Overhead Counterpoise Systems (OCS), OCS, 580mm CEILING MOUNT, PORTEGRA2, Catalog # OCS CEIL 58, Material Number 84433765 |
| Product code | JAK |
| Recalling firm | Bayer Medical Care, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 26, 2018 |
| 510(k) numbers | K934206 |
| FEI number | 2520313 |
At a glance
- 1–9 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