Atlas FDA

The product is a mobile 3-wheeled electric scooter, model HMV 220. The product contains either a red or blue base. The r

FDA device recall Z-0521-06 · posted 2006-02-16 · Terminated

Recall details

Recalling firm
Tung Keng Enterprise Co., Ltd.
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.
Action taken
The recalling firm sent field correction instructions to their customers on or about 11/1/05.
Root cause
Other
Status
Terminated
Product code
INI
Quantity affected
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
Date initiated
2005-11-01
Date posted
2006-02-16
Date terminated
2012-05-08
Location
Hsiang Taichung County, Taiwan

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.

Related 510(k) clearances

RecordFirmDate
BE-MOBILE 3-WHEELED ELECTRIC SCOOTER, MODEL DK S200 (K033240)Tung Keng Enterprise Co., Ltd.2003-12-18