Universal Quick Adjust under the following labels: 1) Aluminum crutch — Class II medical device recall Z-2104-2016
Terminated recall by Medical Depot Inc., reported 2016-07-06, distributed nationwide. Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
| Recall number | Z-2104-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Depot Inc., Port Washington, NY, United States |
| Recall initiated | 2016-02-17 |
| Classified | 2016-06-30 |
| Reported by FDA | 2016-07-06 |
| Terminated | 2018-06-13 |
| Distributed | Nationwide (US) |
| Quantity | 123,125 pairs |
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.
Reason for recall
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2104-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.