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

Recall Z-0453-2024 — NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176

U.S. FDA — Device Enforcement · United Kingdom · 2022-09-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0453-2024
Date of alert
2022-09-13
Country / jurisdiction
United Kingdom
Risk level
Class II
Risk type
recall
Brand
Thor Photomedicine Ltd
Product category
device
Product type
Devices
Reported risk: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
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.

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