FDA Medical Device Recalls (openFDA)
Permobile Inc.: Permobil Chairman 2K powered wheelchair, Model 1280
- Recall number
- Z-0671-03
- Recalling firm
- Permobile Inc.
- Product
- Permobil Chairman 2K powered wheelchair, Model 1280
- Status
- Terminated
- Initiated
- 2003-01-01
- Posted
- 2003-03-21
- Terminated
- 2008-06-25
- Reason
- Incidents were reported where a drive wheel has come off its motor axle, due either to loosening of the wheel bolt or a broken wheel bolt.
- Root cause
- Other
- Action
- Permobil Inc has notified its field representatives of the voluntary recall and these representatives have been provided with lists of each Chairman 2K serial number and the Dealer to which the wheelchair was sold.
- Quantity
- 1582
- Distribution
- Nationwide, Puerto Rico, Canada
- Lot, serial or model codes
- Serial Numbers: 1100068 to 1103702
- 510(k) numbers
- ["K991658"]
- PMA numbers
- not on file
- Product code
- I--TI
- Firm FEI
- 1221084
- Firm city
- Lebanon
- Firm state
- TN
- 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