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

Recall Z-0458-2025 — MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 720001F0

U.S. FDA — Device Enforcement · United States · 2024-10-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0458-2025
Date of alert
2024-10-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Getinge Usa Sales Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04046768136793
Reported risk: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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