Device recall
Z-2105-2016: Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1…
FDA device recall · Class II · Medical Depot Inc.
Key facts
| Recall number (Z-number) | Z-2105-2016 |
|---|---|
| Recall event | 73918 |
| Product | Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg. |
| Product code | INP |
| Recalling firm | Medical Depot Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2018 |
| FEI number | 3002997602 |
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