FDA Medical Device Recalls (openFDA)
Sunrise Medical (US) LLC: Sunrise Medical Zippie TS wheelchair To empower physically challenged person by providing a means or mobility.
- Recall number
- Z-1103-2012
- Recalling firm
- Sunrise Medical (US) LLC
- Product
- Sunrise Medical Zippie TS wheelchair To empower physically challenged person by providing a means or mobility.
- Status
- Terminated
- Initiated
- 2012-01-13
- Posted
- 2012-02-24
- Terminated
- 2012-02-27
- Reason
- One Zippie TS Wheelchair was made per customer order was shipped with transit brackets for use a seat in a motor vehicle, however the chair was not configured with a back tested seat for motor vehicle use.
- Root cause
- Employee error
- Action
- Sunrise Medical contacted customer by telephone on January 17, 2012 to arrange for removal of transit brackets. The Sunrise Sales rep then visited the customers on January 18, 2012 and removed the bracket from the chair making it appropriate for intended use. If you need any additional information or have any questions, call 559-348-2572 or email: laurie.roberts@sunmed.com.
- Quantity
- 1 chair
- Distribution
- Nationwide distribution: OK only.
- Lot, serial or model codes
- Model number: E1Z1A; Serial number: Z1SE-006474.
- 510(k) numbers
- ["K973673"]
- PMA numbers
- not on file
- Product code
- IOR
- 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