FDA Device recall Z-2104-2016
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per c…
- FDA Device
- Class II
- terminated
- Published 2016-07-06
On 2016-07-06 the FDA classified a Class II recall of Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per c… by Medical Depot, citing tip crutch failure involving the bottom of the metal portion which comes in contact with ground.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2104-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-02-17 |
| Published | 2016-07-06 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medical Depot |
| Distribution | US |
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
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Identifiers
| code_info | Item #: 1) RTL 10400, 2) RTL 10402 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2104-2016%22
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