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

Recall Z-0156-2024 — Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085

U.S. FDA — Device Enforcement · United States · 2023-02-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0156-2024
Date of alert
2023-02-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Omega Medical Imaging, Inc.
Product category
device
Product type
Devices
Reported risk: An actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety cable at one location.
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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