CLASS II Device recall · Reported 26 Aug 2020 · FDA Enforcement Report
Golden Technologies Model Number PR515 Lift Chair recalled
Golden Technologies is recalling Golden Technologies. The recall was initiated on 6 Jul 2020 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2817-2020
- FDA event ID
- 86106
- Recalling firm
- Golden Technologies, Old Forge, PA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Jul 2020
- FDA classified
- 17 Aug 2020
- Reported
- 26 Aug 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 6 Jul 2020 | Recall initiated by company | |
| 17 Aug 2020 | Classified by FDA | +42 days |
| 26 Aug 2020 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Suspect poor weld on back KD bar.
Product as listed by the FDA
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.
Where it was distributed
US Only
Questions about this recall
Is Golden Technologies Model Number PR515 Lift Chair - Product Usage: is recalled?
Yes. Golden Technologies recalled Golden Technologies Model Number PR515 Lift Chair - Product Usage: is on 6 Jul 2020. The recall is Class II and its status is Terminated. Recall number Z-2817-2020.
Why was it recalled?
Suspect poor weld on back KD bar.
Which lots are affected?
Model Number - PR515 Unique Device Identifier (UDI) - B247PR515
Where was it sold?
US Only
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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