Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2817-2020 — 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.

U.S. FDA — Device Enforcement · United States · 2020-07-06 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2817-2020
Date of alert: 2020-07-06
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Golden Technologies, Inc.
Product category: device
Product type: Devices

Reported risk: Suspect poor weld on back KD bar.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2817-2020 — 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.

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