Getinge Usa Sales Inc: Device Recall

Recall #Z-0457-2025 · 10/03/2024

Class II: Risk

Recall Details

Recall Number
Z-0457-2025
Classification
Class II
Product Type
Device
Recalling Firm
Getinge Usa Sales Inc
Status
Ongoing
Date Initiated
10/03/2024
Location
Wayne, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
234 units

Reason for Recall

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

Product Description

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: 720001B2

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, France, Germany, Greece, India, Israel, Japan, Jordan, Korea, Republic Of Kuwait, "Macedonia, The Former Yugoslav Republic Of", Malaysia, Mauritius, Mexico, Montenegro, Netherlands, New Zealand, Panama, Peru, Portugal, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Viet Nam.

Other Recalls by Getinge Usa Sales Inc

View all recalls by Getinge Usa Sales Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.