FDA Medical Device Recalls (openFDA)
Golden Technologies, Inc.: Buzzaround XL scooters' Product Usage: mobility
- Recall number
- Z-1235-2014
- Recalling firm
- Golden Technologies, Inc.
- Product
- Buzzaround XL scooters' Product Usage: mobility
- Status
- Terminated
- Initiated
- 2014-01-21
- Posted
- 2014-03-20
- Terminated
- 2015-07-23
- Reason
- 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.
- Root cause
- Device Design
- 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.
- Quantity
- 5044
- Distribution
- Worldwide Distribution - USA Nationwide
- Lot, serial or model codes
- GB 116 and GB146 series, with multiple serial numbers
- 510(k) numbers
- ["K041025"]
- PMA numbers
- not on file
- Product code
- INI
- Firm FEI
- 2523955
- Firm city
- Old Forge
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28