Device recall
Z-0959-05: Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery…
FDA device recall · Class II · Motion Control, Inc.
Key facts
| Recall number (Z-number) | Z-0959-05 |
|---|---|
| Recall event | 32060 |
| Product | Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis. |
| Product code | IQZ |
| Recalling firm | Motion Control, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2008 |
| FEI number | 3001237006 |
At a glance
- None 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