FDA Device recall Z-2103-2016
Universal aluminum crutch, 1 pair per case Aid the user in walking while relieving weight from one foot or leg
- FDA Device
- Class II
- terminated
- Published 2016-07-06
On 2016-07-06 the FDA classified a Class II recall of Universal aluminum crutch, 1 pair per case Aid the user in walking while relieving weight from one foot or leg 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-2103-2016 |
| 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 aluminum crutch, 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 #: RTL 10433 |
|---|
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-2103-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.