Maquet recalls Meera Mobile Operating Tables with specific serial numbers due to risk of electric shock from exposed components. Affected models include Part 720001B2, B0, F2, F0, and 710001B2/B0/F0.
User may suffer an electric shock when coming in contact with the exposed electronic components
Maquet is recalling specific models of Meera Mobile Operating Tables because exposed electronic components could cause electric shock if touched. This affects medical devices used in surgeries and patient care settings.
The tables have exposed electronic components that can cause electric shock if a person comes into contact with them. This hazard occurs during normal use when the table is being handled or adjusted.
Healthcare professionals and patients using the Meera Mobile Operating Tables in medical facilities are most at risk. The recall applies to specific serial number ranges for each model.
Check the serial number on the table's label. Affected models include Part 720001B2 (SN 1-416 and 417-503), Part 720001B0 (SN 1-1416), Part 720001F2 (SN 1-91), Part 720001F0 (SN 1-220), and Part 710001B2/B0/F0 with specific serial ranges.
Identify the serial number on the table's label to determine if it falls within the affected ranges listed in the recall notice.
The Meera Mobile Operating Tables have exposed electronic components that could cause electric shock if touched during normal use.
Affected models include Part 720001B2 (SN 1-416 and 417-503), Part 720001B0 (SN 1-1416), Part 720001F2 (SN 1-91), Part 720001F0 (SN 1-220), and Part 710001B2/B0/F0 with specific serial numbers.
No, but you should check the serial number to see if your table is affected. If it is, contact Maquet for further instructions.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1734-2019 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1734-2019 from Maquet. 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.
