The product is a mobile 3-wheeled electric scooter, model HMV 220. The product contains either a red or blue base. The red base is identified with SKU #9153641905. The blue base is identified with SKU #9153641906. The product is distributed by the Invacare Corporation.
FDA Recall Z-0521-06 · Posted 2006-02-16
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Recalling FirmTung Keng Enterprise Co., Ltd.
Recall StatusTerminated
Product CodeINI
Date Initiated2005-11-01
Date Terminated2012-05-08
Product Quantity8,213 total devices
Reason for Recall
The throttle spring, located in the hand throttle assembly, can fracture, resulting in the scooter not stopping when the user releases the throttle.
Firm Action
The recalling firm sent field correction instructions to their customers on or about 11/1/05.
Root Cause
Other
Distribution Pattern
The product was distributed to OHL/Invacare, Rancho Technology Park Bldg. B 8950, Rancho Cucamonga, CA 91730; OHL/Invacare, 1100 Whitaker Road, Plainfield, IN 46168; Invacare Corporation, 39400 Taylor Parkway North Ridgeville, OH 44039; and Invacare, Dallas Texas Distribution Center, 3460 South Watson Rd., Arlington, TX 76014.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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