Getinge recalls MEERA CL mobile operating tables with error code 50037 that may cause procedural delays during patient positioning. 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 delay critical medical procedures if the table stops moving during patient positioning.
The MEERA table may stop moving unexpectedly when controlled via IR-Hand Control, causing procedural delays. This error code 50:037 occurs sporadically and may interrupt patient positioning during surgery or medical procedures.
Healthcare professionals using MEERA CL mobile operating tables for patient positioning during surgery or procedures are most at risk. Patients receiving care during these procedures may be affected if delays occur.
Check for the item number 700001B0 and serial numbers starting with 491-603 on the table. The recall applies to MEERA CL mobile operating tables used in medical settings.
Look for error code 50037 on the IR-Hand Control when moving the table. If this error occurs, the table may stop moving unexpectedly.
The error code 50037 may cause the MEERA table to stop moving unexpectedly when controlled via IR-Hand Control, leading to procedural delays during patient positioning.
Check for error code 50037 on the IR-Hand Control. If the error occurs, the table may stop moving unexpectedly. Contact Getinge for further instructions.
The recall record does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0462-2025 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0462-2025 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.
