Sunrise Medical Quickie Power Wheelchairs: Three models -Rhythm, Groove, and Zippy Z-Bop (with Quickie IQ Enhanced Displ
FDA device recall Z-1163-2007 · posted 2007-08-14 · Terminated
Recall details
- Recalling firm
- Sunrise Medical Inc
- Reason for recall
- The wire harness connected to the display housing (Quickie IQ Enhanced Displays) may separate and cause sparks from a short circuit.
- Action taken
- Firm contacted consignees by phone and mailed May 1, 2007, Urgent Medical Device notification letters.
- Root cause
- Component design/selection
- Status
- Terminated
- Product code
- ITI
- Quantity affected
- 229 Enhanced Display units (affecting 220 wheelchairs)
- Distribution
- Product was distributed Worldwide.
- Date initiated
- 2007-04-23
- Date posted
- 2007-08-14
- Date terminated
- 2008-03-25
- Location
- Fresno, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| QUICKIE RHYTHM & GROOVE SERIES POWER WHEELCHAIRS W/QUICKIE DELPHI CONTROLS (K060531) | Sunrise Medical | 2006-03-17 |