Class II — Sunrise Medical (US) LLC
| Recalling firm | Sunrise Medical International Inc. |
|---|---|
| Registered facility | SUNRISE MEDICAL INTERNATIONAL INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| 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. |
| Quantity | 14, 035 |
| Distribution | Worldwide Distribution - US (nationwide) and the countries of Argentina, Brazil, Columbia, Costa Rica, Mexico, Panama, Uruguay and Venezuela. |
| Initiated | 2012-06-26 |
| Classified | 2012-07-31 |
| Terminated | 2012-11-01 |
| Recall number | Z-2113-2012 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sunrise Medical (US) LLC (Z-2113-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/62493/
Alerts for Sunrise Medical International Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.