Z-0522-06

The product is a mobile 3-wheeled electric scooter, model HMV 250. The product contains either a red or blue...

Name: Z-0522-06 The product is a mobile 3-wheeled electric scooter, model HMV 250. The product contains either a red or blue...
Creator: Tung Keng Enterprise Co., Ltd.
Published: 2005-11-01
License: https://open.fda.gov/license/

Tung Keng Enterprise Co., Ltd. / initiated 2005-11-01 / Terminated

FDA source

Tung Keng Enterprise Co., Ltd. began a recall of The product is a mobile 3-wheeled electric scooter, model HMV 250. The product contains either a red or blue base. The red base is identified with SKU... on 2005-11-01. The reason FDA records is "The throttle spring, located in the hand throttle assembly, can fracture, resulting in the scooter not stopping when the user releases the throttle". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0522-06
Status: Terminated
Initiated: 2005-11-01
Posted: 2006-02-16
Terminated: 2012-05-08
Recalling firm: Tung Keng Enterprise Co., Ltd.
Product: The product is a mobile 3-wheeled electric scooter, model HMV 250. The product contains either a red or blue base. The red base is identified with SKU #915363224. The blue base is identified with SKU #915363225. The product is distributed by the Invacare Corporation.
Product code: INI Vehicle, Motorized 3-Wheeled
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.
FDA root cause: Other
Action: The recalling firm sent field correction instructions to their customers on or about 11/1/05.
Quantity in commerce: 8,213 total devices
Distribution: 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.
Product codes and lots: All serial numbers 04H86001 to 05A468246.

Product code INI

K033240Class IIBe-Mobile 3-Wheeled Electric Scooter, Model Dk S200Tung Keng Enterprise Co., Ltd. / cleared 2003-12-18

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)