Buzzaround XL scooters' Product Usage: mobility
FDA Recall Z-1235-2014 · Posted 2014-03-20
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Recalling FirmGolden Technologies, Inc.
Recall StatusTerminated
Product CodeINI
Date Initiated2014-01-21
Date Terminated2015-07-23
Product Quantity5044
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.
Firm Action
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
Distribution Pattern
Worldwide Distribution - USA Nationwide
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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