Getinge recalls MEERA CL mobile operating tables that may stop unexpectedly due to error code 50037, causing procedural delays during surgery. 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 operations.
The table may stop moving unexpectedly when controlled via IR-Hand Control, causing procedural delays. This error code 50037 occurs sporadically and could interrupt surgical procedures if the table stops during critical operations.
Healthcare professionals using MEERA CL mobile operating tables for surgical procedures are most at risk. Patients undergoing surgery may experience delays if the table stops unexpectedly during critical steps.
Check for item number 700001F0 and serial number 9 on the table. The recall applies to MEERA CL mobile operating tables used in surgical settings.
Look for error code 50037 on the IR-Hand Control when the table stops moving unexpectedly.
The recall indicates a potential for procedural delays during surgery, but does not mention risk of injury or serious harm.
Check for item number 70001F0 and serial number 9 on the table. The recall applies to MEERA CL mobile operating tables used in surgical settings.
The recall does not specify a remedy, so no action is required beyond checking for the error code and ensuring the table is used with proper controls.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0463-2025 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0463-2025 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.
