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

Recall Z-0365-2023 — FULL VISION INC. TRACKMASTER,TREADMILL TMX428 220V, Model #317-07927

U.S. FDA — Device Enforcement · United States · 2022-08-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0365-2023
Date of alert
2022-08-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Full Vision Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00860176000613
Reported risk: This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety Tether, that when the magnet is pulled loose as during a fall, the treadmill may fail to stop.
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.