Device recall
Z-1198-2017: Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The…
FDA device recall · Class II · Allen Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1198-2017 |
|---|---|
| Recall event | 76257 |
| Product | Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder Positioner is intended to allow for the controlled manipulation of the arm and shoulder joint during arthroscopic surgical procedures. |
| Product code | HST |
| Recalling firm | Allen Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 3, 2018 |
| FEI number | 1221538 |
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