Zippie IRIS Wheelchair — Class II medical device recall Z-2466-2015
Terminated recall by Sunrise Medical (US) LLC, reported 2015-09-02, distributed nationwide. Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest System with Dynamic Backrest may bre
| Recall number | Z-2466-2015 |
|---|---|
| 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 | 2015-07-27 |
| Classified | 2015-08-26 |
| Reported by FDA | 2015-09-02 |
| Terminated | 2015-12-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE |
| Quantity | 64 wheelchairs |
| Reason classes | device malfunction |
| Model numbers | EIZ51, EIZ5A |
Product
Zippie IRIS Wheelchair. model EIZ5A in combination with option code 188M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
Reason for recall
Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest System with Dynamic Backrest may break over time resulting in a fall or injury to occupant.
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-2466-2015. 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.