FDA Medical Device Recalls (openFDA)
Invacare Corporation: 3G Storm Series Power Wheelchair with Power Tilt Option.
- Recall number
- Z-0303-06
- Recalling firm
- Invacare Corporation
- Product
- 3G Storm Series Power Wheelchair with Power Tilt Option.
- Status
- Terminated
- Initiated
- 2005-10-11
- Posted
- 2005-12-23
- Terminated
- 2012-04-12
- Reason
- When the powered seating system is tilted completely in the rearward position, a potential pinch point is created between the seat and the seat frame.
- Root cause
- Other
- Action
- The recalling firm sent letters to all consignees.
- Quantity
- 16 devices
- Distribution
- The product was sent to distributors located in AL, GA, CA, IL, KS, MN, NC, PA, TX, and VA.
- Lot, serial or model codes
- Serial numbers: 05G066858, 05G066859, 05G071801, 05G071803, 05G077773, 05G079666, 05G089011, 05G089012, 05G092274, 05G105434, 05G106984, 05G111332, 05G117359, 05G121857, 05G125563, 05H144898
- 510(k) numbers
- ["K001777","K993413"]
- 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