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FDA Medical Device Recalls (openFDA)

Electric Mobility Corp: Rascal 600F and 600T scooters, unspecified power wheelchair.

Recall number
Z-0903-06
Recalling firm
Electric Mobility Corp
Product
Rascal 600F and 600T scooters, unspecified power wheelchair.
Status
Terminated
Initiated
2006-04-17
Posted
2006-05-24
Terminated
2014-04-08
Reason
The four seat mast mounting screws can loosen, causing seat to wobble. The chair seat actuator and portions of the seat can malfunction and/or break. Firm is aware of problems with the seat and injuries sustained from the powered wheelchair/scooter seat malfunction. Firm has not initiated recall, claims it is a Warranty Advisory.
Root cause
Other
Action
At this point, the firm has committed to send out a Warranty advisory. No recall has been initiated.
Quantity
12,220 chairs
Distribution
To customers nationwide.
Lot, serial or model codes
Numerous serial numbers
510(k) numbers
["K002616","K924515","K972370"]
PMA numbers
not on file
Product code
ITI
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

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