Class II — Medical Depot Inc.
| Recalling firm | Medical Depot, Inc DBA Drive DeVilbiss Healthcare |
|---|---|
| Registered facility | AmFab Co., LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| Product | EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ adjust aluminum crutch, tall adult, 1 pair per case & 6) EZ adjust aluminum crutch, tall adult, 8 pairs per case |
| Quantity | 123,125 pairs |
| Distribution | Nationwide Distribution |
| Initiated | 2016-02-17 |
| Classified | 2016-06-30 |
| Terminated | 2018-06-13 |
| Recall number | Z-2102-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medical Depot Inc. (Z-2102-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73918/
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