Device recall
Z-1594-2021: Alpha Interlock Suspension System Lanyard Body: An external prosthetic device…
FDA device recall · Class II · WillowWood Global Llc
Key facts
| Recall number (Z-number) | Z-1594-2021 |
|---|---|
| Recall event | 87825 |
| Product | Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with a one-way air expulsion valve plus a locking mechanism. Product design features an easy release mechanism. Available with or without a titanium pyramid. The lanyard is part of the… |
| Product code | IPM |
| Recalling firm | WillowWood Global Llc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1522166 |
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