Recall Z-2817-2020— Golden Technologies, Inc.

Name: FDA recall Z-2817-2020
Creator: U.S. Food and Drug Administration
Published: 2020-07-06

Class II · Terminated

Class II FDA medical device recall by Golden Technologies, Inc., initiated 2020-07-06, terminated 2021-06-21. It names one FDA 510(k) clearance: K880800. Product: Golden Technologies Model Number PR515 Lift Chair - Product Usage: is to provide lift assistance for persons who have difficulty rising from a seated position to a standing position.. Reason: Suspect poor weld on back KD bar..

Recalling firm: Golden Technologies, Inc.
Classification: Class II
Status: Terminated
Initiated: 2020-07-06
Terminated: 2021-06-21
Firm location: Old Forge, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K880800 — GOLDEN POWER LIFT CHAIRGolden Technologies, Inc.·cleared 1988-03-14

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

Golden Technologies Model Number PR515 Lift Chair - Product Usage: is to provide lift assistance for persons who have difficulty rising from a seated position to a standing position.

Reason for recall

Suspect poor weld on back KD bar.

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