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Electric Mobility Rascal

by Electric Mobility Corp. 510(k)

Active United States

510(k) K924515

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK924515 Date28 Mar 1994DecidedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

6 recalls · FDA

    • Terminated Z-0175-2008 FDA Unclassified (pre-2012) initiated 29 Mar 2007

    Seat and/or lift actuator problems: 1) Models equipped with a Seat Lift, the mast screw and washer holding the Seat Lift Actuator in place will loosen break off or fall out; 2) Models assembled with Seat Lift Actuator or Seat Post Mounting Bolts, the seat may wobble or the seat will break off from the vehicle; 3) Models using Seat-On Lifting brackets with a hoist to raise an EMC vehicle equipped w

    • Terminated Z-0174-2008 FDA Unclassified (pre-2012) initiated 22 Mar 2007

    Seat and/or lift actuator problems: 1) Models equipped with a Seat Lift, the mast screw and washer holding the Seat Lift Actuator in place will loosen break off or fall out; 2) Models assembled with Seat Lift Actuator or Seat Post Mounting Bolts, the seat may wobble or the seat will break off from the vehicle; 3) Models using Seat-On Lifting brackets with a hoist to raise an EMC vehicle equipped

    • Terminated Z-0903-06 FDA Unclassified (pre-2012) initiated 17 Apr 2006 on shared 510(k) K924515

    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.

    • Terminated Z-1376-05 FDA Unclassified (pre-2012) initiated 5 May 2005 on shared 510(k) K924515

    The engager set screw may become loose. This problem may cause the potentiometer to become off-center thus affecting the end users stopping capabilities.

  • 2 recalls, same reason

    • Terminated Z-0910-03 FDA Unclassified (pre-2012) initiated 7 Feb 2003
    • Terminated Z-0909-03 FDA Unclassified (pre-2012) initiated 7 Feb 2003

    The plastic tires may shatter if the tire is over-inflated and could cause serious injury.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Specification

510(k)

510(k) Number
FDA Product Code
INI
FDA applicant
Electric Mobility, LLC
Device Class
Class II
Regulation
21 CFR Part 890.3800
Advisory Committee
Physical Medicine
FDA Decision
SN

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