FDA Medical Device Recalls (openFDA)
Invacare Corporation: Pronto M51 Wheelchair, component- seat
- Recall number
- Z-1400-06
- Recalling firm
- Invacare Corporation
- Product
- Pronto M51 Wheelchair, component- seat
- Status
- Terminated
- Initiated
- 2006-06-14
- Posted
- 2006-08-10
- Terminated
- 2007-08-22
- Reason
- Some of the wheelchairs were distributed with seats that did not have a seat positioning strap.
- Root cause
- Other
- Action
- The recalling firm sent a recall letter, dated 06/06 to consignees.
- Quantity
- 853 units
- Distribution
- Nationwide.
- Lot, serial or model codes
- There is no code on the individual seat. Recall covers seats on wheelchairs distributed between 03/14/2006 and 04/07/2006.
- 510(k) numbers
- ["K021680"]
- PMA numbers
- not on file
- Product code
- ITI
- Firm FEI
- 3002889431
- Firm city
- Elyria
- Firm state
- OH
- 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