FDAClass IINovember 20, 2024

MEERA CL mobile operating table - Designed for the recall

MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical…

Why was MEERA CL mobile operating table - Designed for the recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 04046768136304 S/N: 252 - 254

Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical…
Recalling firm
Getinge Usa Sales Inc
Quantity
3 units
Distribution
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.
Recall date
November 20, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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