Use cautionMedical device recall · FDA · Published September 6, 2023
Getinge Meera Mobile Operating Table Recall: Risk of Unintended Patient Movement During
Getinge recalls Meera Mobile Operating Tables with model 7200.01F2 that may unintentionally move patients during surgery due to a control unit issue, posing potential injury risks.
Under certain conditions, an issue might prevent the device from performing as intended. A specific sequence of commands on the control unit activates the traction drive and triggers an unintended driving (autodrive) of max. 7 sec. may result in the following reasonably foreseeable injury or damage to the health of patients and/or users
Take action
Contact the company
📍Recalling firmGetinge Usa Sales Inc1 Geoffrey Way · Wayne, NJ 07470-2035
“Getinge Meera Mobile Operating Table Recall: Risk of Unintended Patient Movement During.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57380-getinge-meera-mobile-operating-table-recall-risk-of-unintended-patient. Based on FDA recall #Z-0036-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0036-2024%22&limit=1).
Getinge Usa Sales Inc recalled Meera Mobile Operating Tables on Sept. 6, 2023, according to the FDA. The devices may unexpectedly drive for up to seven seconds due to a control unit issue. This Class II recall affects 224 units distributed nationwide.
According to the FDA, a specific sequence of commands on the control unit may activate the traction drive and trigger an unintended driving of up to seven seconds. This issue might prevent the device from performing as intended under certain conditions. The agency states this could result in reasonably foreseeable injury or damage to the health of patients and/or users.
Context
GovInfoNow's records show Getinge Usa Sales Inc has had 16 other recalls on record since Dec. 9, 2021. Other recent recalls of similar products include Getinge MEERA CL Mobile Operating Table Recall (Oct. 3, 2024) and Getinge ALPHAMAXX Mobile Operating Table Charger Recall (May 29, 2024). Recent recalls of similar operating tables include Philips Azurion 7 B20 System Recall (Jan. 26, 2026), IMRIS ORT300 Operating Room Table Recall (Aug. 6, 2026), and Philips Azurion 3 M15 System Recall (Jan. 26, 2026).
How to tell if you have this one
Check for model number 7200.01F2 on the device. The serial numbers follow a specific pattern starting with '7 10 9 18...' as listed in the recall notice.
Brand
Getinge
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Model
Verify the model number is 7200.01F2 to confirm if the device is affected.
Stop Using Immediately
If the model number matches, stop using the table until a fix is implemented to prevent unintended movement.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 35 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-0036-2024 (September 6, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0036-2024 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.