Atlas FDA

Buzzaround XL scooters' Product Usage: mobility

FDA device recall Z-1235-2014 · posted 2014-03-20 · Terminated

Recall details

Recalling firm
Golden Technologies, Inc.
Reason for recall
Buzzaround XL scooters' front to rear lockup can become unintentionally disengaged due to possible improper fit of the front alignment cup to the rear alignment screw.
Action taken
Golden Technologies sent a recall notification letter, dated January 14, 2014 to providers/dealers. A second letter, dated January 21, 2014 was sent to these same customers. Based on a slow initial response, the firm intends to send out the correction kit with the inspection acknowledgement form as soon as possible. Based on the overall response from dealers, a third consumer letter was drafted (notification3) for mailing directly to known consumers, if necessary. For help contact a special technical service hotline at 1-800-624-6374 ext. 392.
Root cause
Device Design
Status
Terminated
Product code
INI
Quantity affected
5044
Distribution
Worldwide Distribution - USA Nationwide
Date initiated
2014-01-21
Date posted
2014-03-20
Date terminated
2015-07-23
Location
Old Forge, PA

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Related 510(k) clearances

RecordFirmDate
BUZZAROUND, VEHICLE, MOTORIZED 3-WHEELED (K041025)Golden Technologies, Inc.2004-05-03