Recall Z-1235-2014— Golden Technologies, Inc.

Name: FDA recall Z-1235-2014
Creator: U.S. Food and Drug Administration
Published: 2014-01-21

Class II · Terminated

Class II FDA medical device recall by Golden Technologies, Inc., initiated 2014-01-21, terminated 2015-07-23. It names one FDA 510(k) clearance: K041025. 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..

Recalling firm: Golden Technologies, Inc.
Classification: Class II
Status: Terminated
Initiated: 2014-01-21
Terminated: 2015-07-23
Firm location: Old Forge, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K041025 — BUZZAROUND, VEHICLE, MOTORIZED 3-WHEELEDGolden Technologies, Inc.·cleared 2004-05-03

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.