Padded Swing Away Arm Rest with Receiver — Class II medical device recall Z-2113-2012
Terminated recall by Sunrise Medical (US) LLC, reported 2012-08-08, distributed nationwide. Reports of injury when the Padded Swing Away Armrest is used for full body weight. Owner's manual states that
| Recall number | Z-2113-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sunrise Medical (US) LLC, Fresno, CA, United States |
| Recall initiated | 2012-06-26 |
| Classified | 2012-07-31 |
| Reported by FDA | 2012-08-08 |
| Terminated | 2012-11-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BR, CR, MX, PA, UY, VE |
Product
Padded Swing Away Arm Rest with Receiver; Uses on wheelchair models: Quickie Q7 (EIR4), GT (EIR3), GTi (EIT4) and Zippie Zone (EIRZ1). Product Usage: To empower physically challenged persons by providing a means of mobility. This includes temporary and permanent conditions.
Reason for recall
Reports of injury when the Padded Swing Away Armrest is used for full body weight. Owner's manual states that armrest is only designed for resting of forearm.
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-2113-2012. 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.