FDA Medical Device Recalls (openFDA)
Invacare Corporation: Invacare 2G Tarsys Seating System, Model 2GT.
- Recall number
- Z-0342-04
- Recalling firm
- Invacare Corporation
- Product
- Invacare 2G Tarsys Seating System, Model 2GT.
- Status
- Terminated
- Initiated
- 2003-12-15
- Posted
- 2004-01-14
- Terminated
- 2008-09-13
- Reason
- The weld joints on the seat back may fail and cause possible injury to the patient.
- Root cause
- Other
- Action
- The firm notified their consignees by letter and telephone on 12/15/2003.
- Quantity
- 5,990 units
- Distribution
- The units were shipped to domestic dealerships located nationwide, and to foreign accounts in Canada, China, Oman, and West Indies.
- Lot, serial or model codes
- Serial Numbers: 00Axxx thru 00Lxxx, 01Axxx thru 01Lxxx, and 02Axxx.
- 510(k) numbers
- ["K991119"]
- PMA numbers
- not on file
- Product code
- ITI
- Firm FEI
- 1525712
- 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