Maquet Meera Mobile Operating Table Recall: Electric Shock Hazard
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.
Use caution until it’s fixed
User may suffer an electric shock when coming in contact with the exposed electronic components
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/67950-maquet-meera-mobile-operating-table-recall-electric-shock-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/67950-maquet-meera-mobile-operating-table-recall-electric-shock-hazard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1734-2019
Cite this page
“Maquet Meera Mobile Operating Table Recall: Electric Shock Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67950-maquet-meera-mobile-operating-table-recall-electric-shock-hazard. Based on FDA recall #Z-1734-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1734-2019%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Maquet- Category
Medical device
What to do — step by step
Check Serial Numbers
Identify the serial number on the table's label to determine if it falls within the affected ranges listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide - US Nationwide Distribution Foreign: ALGERIA ANGOLA ARGENTINA AUSTRALIA AUSTRIA BAHRAIN BANGLADESH BELGIUM BOLIVIA BOTSWANA BOSNIA AND HERZEGOVINA BRAZIL BULGARIA CANADA CHILE CHINA COLOMBIA COSTA RICA CROATIA CZECH REPUBLIC…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 3.2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
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.
- Official source: FDA Recall #Z-1734-2019 (May 6, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1734-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.