FDA Medical Device Recalls (openFDA)
Electric Mobility Corp: Rascal LiteWay 214 manufactured by Giant Manufacturing, Taiwan.
- Recall number
- Z-0415-2011
- Recalling firm
- Electric Mobility Corp
- Product
- Rascal LiteWay 214 manufactured by Giant Manufacturing, Taiwan.
- Status
- Terminated
- Initiated
- 2010-09-27
- Posted
- 2010-11-18
- Terminated
- 2014-04-03
- Reason
- Scooter seat bases were found to have insufficient welding which may lead to the seat base becoming loose and causing the seat to wobble. This may result in complete failure of the seat base, causing the user to fall off the vehicle.
- Root cause
- Device Design
- Action
- The Rascal Company (Electric Mobility Corporation) sent Urgent Medical Device Recall Notice Scooter Seat Base letters dated October 7, 2010 and November 11, 2010 letter to their affected retail customers and affected dealers. The letter instructs the reader that the seat base may become loose, causing the seat to wobble and if not replaced the wobble could lead to a complete failure of the seat base and cause an individual to fall off their vehicle and become injured. The letters also instruct the reader to replace seat bases immediately. Respone forms are attached. Seats with new seat bases will be shipped with return shipping labels to return the original base to the factory. Service representatives will replace the seat base for customers. Customers can contact the Rascal Company about this recall at 1-800-662-4548.
- Quantity
- 172 units
- Distribution
- Worldwide Distribution: Throughout the US and Canada
- Lot, serial or model codes
- No expiration date; 510 K - K002616; Device Listing #E394292; LW214, EMC Part #43062400, EMC Part #43062500 LW3 Plus, EMC Part #43062600 LW3x6, EMC Part #43062800
- 510(k) numbers
- ["K002616"]
- PMA numbers
- not on file
- Product code
- INI
- Firm FEI
- 2246975
- Firm city
- Sewell
- Firm state
- NJ
- 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