ReTurn 7500/7500 Aid — Class II medical device recall Z-0303-2017
Terminated recall by Handicare USA, Inc., reported 2016-11-02, distributed in CT, IL, ME, NE, NJ, NV, NY, PA. During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, aft
| Recall number | Z-0303-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Handicare USA, Inc., Allentown, PA, United States |
| Recall initiated | 2014-04-15 |
| Classified | 2016-10-24 |
| Reported by FDA | 2016-11-02 |
| Terminated | 2016-12-13 |
| Distributed | CT, IL, ME, NE, NJ, NV, NY, PA |
| Serial numbers | 073317697400500012, 073317697400500057, 373317697270501334, 373317697270501430 |
| Model numbers | 7322, 7400, 7500 |
Product
ReTurn 7500/7500 Aid, transfer
Reason for recall
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.
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-0303-2017. 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.