Z-2817-2020 Class II Terminated

Recalled by Golden Technologies, Inc. — Old Forge, PA

FDA device recall Z-2817-2020 was initiated by Golden Technologies, Inc. on July 6, 2020 and is designated Class II. Reason for recall: Suspect poor weld on back KD bar. The recall status is terminated (terminated June 21, 2021). Affected quantity: 251.

Recall Details

Product Type
Devices
Report Date
August 26, 2020
Initiation Date
July 6, 2020
Termination Date
June 21, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
251

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.

Distribution Pattern

US Only

Code Information

Model Number - PR515 Unique Device Identifier (UDI) - B247PR515