Getinge recalls MEERA CL mobile operating tables with error code 50037 that may stop movement during use, causing procedural delays. Affected units have specific serial numbers and item numbers.
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
Getinge is recalling MEERA CL mobile operating tables that may stop moving unexpectedly when controlled via IR-Hand Control, causing procedural delays. This could lead to delays in medical procedures if the table stops during critical tasks.
The error code 50037 occurs sporadically when the table is controlled by an IR-Hand Control, causing the table to stop moving. This can lead to procedural delays during critical medical tasks, but does not cause injury or damage to the table.
Healthcare professionals using MEERA CL mobile operating tables for surgical procedures or patient care are most at risk. Patients and staff during medical interventions may be affected if the table stops unexpectedly.
Check for the item number 720001B2 and serial numbers 10894-11128 on the table. The product was sold with specific UDI-DI: 04046768124349.
Look for error code 50037 on the IR-Hand Control when the table is being operated.
The recall record states the error may cause procedural delays but does not mention injury risks.
Check for item number 720001B2 and serial numbers 10894-11128 on the table.
The recall record does not specify a remedy, so no action is required beyond checking for the error code.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0457-2025 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0457-2025 from Getinge. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
