Buzzaround XL scooters' Product Usage: mobility — Class II medical device recall Z-1235-2014
Terminated recall by Golden Technologies, Inc., reported 2014-03-26, distributed nationwide. Buzzaround XL scooters' front to rear lockup can become unintentionally disengaged due to possible improper fi
| Recall number | Z-1235-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Golden Technologies, Inc., Old Forge, PA, United States |
| Recall initiated | 2014-01-21 |
| Classified | 2014-03-19 |
| Reported by FDA | 2014-03-26 |
| Terminated | 2015-07-23 |
| Distributed | Nationwide (US) |
| Quantity | 5,044 |
Product
Buzzaround XL scooters' Product Usage: mobility
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1235-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.