FDA Medical Device Recalls (openFDA)
Action Products Incorporated: Xact(tm) Drop Seat Base, a plastic seat support in Xact (tm) Integrated and Xact Individual w/ Drop seat Base Wheelchair cushions.
- Recall number
- Z-0709-04
- Recalling firm
- Action Products Incorporated
- Product
- Xact(tm) Drop Seat Base, a plastic seat support in Xact (tm) Integrated and Xact Individual w/ Drop seat Base Wheelchair cushions.
- Status
- Terminated
- Initiated
- 2004-02-02
- Posted
- 2004-07-20
- Terminated
- 2004-09-21
- Reason
- Wheelchair seat may not properly support the user due to cracks in the plastic seat base.
- Root cause
- Other
- Action
- The recalling firm notified dealers by certified letter on 1/19/03. The notification was flagged Attention:Product Recall and advised of seat base susceptibility to cracks and breakage. Dealers were intructed to respond with end user information. Dealers were also provided instructions and materials for crossbar and safety lock installation used with the drop seat bases. Dealers were additionally instructed to forward the provided notification letters to end users.
- Quantity
- 389 wheelchairs
- Distribution
- Product was sold to medical device dealers, primarily pharmacies, nationwide and internationally.
- Lot, serial or model codes
- Drop seat bases are not labeled with serial or code numbers, but are found on all wheelchair cushions labeled as Xact Integrated and Xact Individual w/Drop Seat Base.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KNO
- Firm FEI
- 1181047
- Firm city
- Hagerstown
- Firm state
- MD
- 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