FDA Device recall Z-0303-2017
ReTurn 7500/7500 Aid, transfer
- FDA Device
- Class II
- terminated
- Published 2016-11-02
On 2016-11-02 the FDA classified a Class II recall of ReTurn 7500/7500 Aid, transfer by Handicare Usa, citing during the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount o….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0303-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-15 |
| Published | 2016-11-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Handicare Usa |
| Distribution | CT, IL, ME, NE, NJ, NV, NY, PA |
Product
ReTurn 7500/7500 Aid, transfer
Reason
During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, which in turn results in high load at the attachment holes of the ladder. Eventually, this may cause mechanical fatigue in the material of the ladder.
Identifiers
| code_info | Model # 7400, 7500 and 7322 (spare part) Serial # 373317697270501334, 373317697270501430, 073317697400500012, 073317697400500057 |
|---|
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-0303-2017%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.