Z-2817-2020Class II

Golden Technologies Model Number PR515 Lift Chair -

Name: Z-2817-2020 Golden Technologies Model Number PR515 Lift Chair -
Creator: Golden Technologies, Inc.
Published: 2020-07-06
License: https://open.fda.gov/license/

Golden Technologies, Inc / initiated 2020-07-06 / Terminated / root cause: design

FDA source

Golden Technologies, Inc. began a recall of Golden Technologies Model Number PR515 Lift Chair - Product Usage: is to provide lift assistance for persons who have difficulty rising from a seated position... on 2020-07-06. FDA classified it as Class II and gives the reason as "Suspect poor weld on back KD bar". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2817-2020
Classification: Class II
Status: Terminated
Initiated: 2020-07-06
Posted: 2020-08-17
Terminated: 2021-06-21
Recalling firm: Golden Technologies, Inc
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.
Product code: INO Chair, Positioning, Electric
Reason for recall: Suspect poor weld on back KD bar.
Root cause tag: design
FDA root cause: Device Design
Action: Golden Tech plans on contacting dealers and internet sellers to inform them of the recall. The firm will provide replacement parts and credit for installation labor compensation.
Quantity in commerce: 251
Distribution: US Only
Product codes and lots: Model Number - PR515 Unique Device Identifier (UDI) - B247PR515

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2817-2020
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2817-2020	Class II	Terminated	Voluntary: Firm initiated	2020-08-26	2020-08-17

Product code INO

K880800Class IIGolden Power Lift ChairGolden Technologies, Inc. / cleared 1988-03-14

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)