FDA Device recall Z-1235-2014
Buzzaround XL scooters' Product Usage: mobility
- FDA Device
- Class II
- terminated
- Published 2014-03-26
On 2014-03-26 the FDA classified a Class II recall of Buzzaround XL scooters' Product Usage: mobility by Golden Technologies, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1235-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-01-21 |
| Published | 2014-03-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Golden Technologies |
| Distribution | US |
Product
Buzzaround XL scooters' Product Usage: mobility
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.
Identifiers
| code_info | GB 116 and GB146 series, with multiple serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1235-2014%22
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