FDA Medical Device Recalls (openFDA)
Sunrise Medical Inc: Sunrise Medical Quickie Power Wheelchairs: Three models -Rhythm, Groove, and Zippy Z-Bop (with Quickie IQ Enhanced Displays)
- Recall number
- Z-1163-2007
- Recalling firm
- Sunrise Medical Inc
- Product
- Sunrise Medical Quickie Power Wheelchairs: Three models -Rhythm, Groove, and Zippy Z-Bop (with Quickie IQ Enhanced Displays)
- Status
- Terminated
- Initiated
- 2007-04-23
- Posted
- 2007-08-14
- Terminated
- 2008-03-25
- Reason
- The wire harness connected to the display housing (Quickie IQ Enhanced Displays) may separate and cause sparks from a short circuit.
- Root cause
- Component design/selection
- Action
- Firm contacted consignees by phone and mailed May 1, 2007, Urgent Medical Device notification letters.
- Quantity
- 229 Enhanced Display units (affecting 220 wheelchairs)
- Distribution
- Product was distributed Worldwide.
- Lot, serial or model codes
- Serial Numbers: USA Rhythm SIN RTM-100023 RTM-100095 RTM-100152 RTM-100278 RTM-100492 RTM-100499 RTM-100510 RTM-100513 RTM-100516 RTM-100597 RTM-100606 RTM-100702 RTM-100703 RTM-100710 RTM-100733 RTM-100823 RTM-100840 RTM-100846 RTM-100854 RTM-101103 RTM-101111 RTM-101112 RTM-101118 RTM-101159 RTM-101166 RTM-101167 RTM-101169 RTM-101174 RTM-101177 RTM-101184 RTM-101188 RTM-101215 RTM-101242 RTM-101252 RTM-101260 RTM-101262 RTM-101264 RTM-101268 RTM-101269 RTM-101271 RTM-101285 RTM-101302 RTM-101309 RTM-101312 RTM-101314 RTM-101347 RTM-101391 RTM-101392 RTM-101394 RTM-101429 RTM-101439 RTM-101464 RTM-101468 RTM-101482 RTM-101548 RTM-101550 RTM-101556 RTM-101562 RTM-101565 RTM-101581 RTM-101588 RTM-101593 RTM-101602 RTM-101649 RTM-101670 RTM-101673 RTM-101689 RTM-101702 RTM-101704 RTM-101720 RTM-101735 RTM-101760 RTM-101761 RTM-101778 RTM-101782 RTM-101798 RTM-101826 RTM-101842 RTM-101854 RTM-101857 RTM-101866 RTM-101867 RTM-101876 RTM-101886 RTM-101892 RTM-101901 RTM-101904 RTM-101911 RTM-101916 RTM-101925 RTM-101941 RTM-101947 RTM-101959 RTM-101974 RTM-101990 RTM-101994 RTM-101997 RTM-102018 RTM-102023 RTM-102024 RTM-102026 RTM-102031 RTM-102033 RTM-102039 RTM-102052 RTM-102053 RTM-102058 RTM-102080 RTM-102081 RTM-102082 RTM-102095 RTM-102106 RTM-102123 RTM-102140 RTM-102144 RTM-102147 RTM-102151 RTM-102153 RTM-102155 RTM-102156 RTM-102164 RTM-102169 RTM-102201 RTM-102204 RTM-102218 RTM-102230 RTM-102237 RTM-102247 RTM-102249 RTM-102253 RTM-102257 RTM-102258 RTM-102264 RTM-102268 RTM-102270 RTM-102271 RTM-102272 RTM-102287 RTM-102298 RTM-102301 RTM-102303 RTM-102315 RTM-102329 RTM-102333 RTM-102344 RTM-102345 RTM-102348 RTM-102363 RTM-102393 RTM-102396 RTM-102397 RTM-102400 RTM-102414 RTM-102429 RTM-102442 RTM-102447 RTM-102462 RTM-102464 RTM-102468 RTM-102474 RTM-102479 RTM-102484 RTM-102490 RTM-102495 RTM-102516 RTM-102523 RTM-102530 RTM-102535 RTM-102571 RTM-102574 RTM-102601 RTM-102602 RTM-102608 RTM-102610 RTM-102611 RTM-102616 RTM-102637 RTM-102639 RTM-102643 RTM-102647 RTM-102659 RTM-137762 Groove S/N GRV-100053 GRV-100059 GRV-100081 GRV-100096 GRV-100203 GRV-100222 GRV-100226 GRV-100228 GRV-100233 GRV-100266 GRV-100267 GRV-100273 GRV-100280 GRV-100287 GRV-100297 GRV-100317 Z-Bop S/N 1 GM01 BB600080 1 GM01 BC600062 1GM01 BC600014 International Rhythm S/N RTM-100516 RTM-100873 RTM-101403 RTM-101423 RTM-101427 RTM-101434 RTM-101580 RTM-101796 RTM-101850 RTM-101954 RTM-101999 RTM-102124 RTM-102129 RTM-102311 RTM-102312 RTM-102376 RTM-OMIT159372 Groove S/N GRV-100166 GRV-100312
- 510(k) numbers
- ["K060531"]
- PMA numbers
- not on file
- Product code
- ITI
- Firm FEI
- 2937137
- Firm city
- Fresno
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28