Agila/Movita/Forta G16805Recalls & reported problems
Drägerwerk AG & Co. KGaA · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048675017684), received between Feb 12, 2024 and Feb 12, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Device Fell1
- Structural Problem1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 12, 2024Structural Problem; Detachment of Device or Device Component; Unintended Movement; Device Fell; Structural Problem; Detachment of Device or Device Component; Unintended Movement; Device Fell
IT WAS REPORTED THAT IN ROOM 366, A DRAWER CAME LOOSE FROM THE COLUMN AND FELL TO THE FLOOR. NO CONSEQUENCES HAVE BEEN REPORTED. HOWEVER, IN CASE OF RECURRANCE IT CANNOT BE EXCLUDED THAT THE PATIENT OR USER WILL BE INJURED BY THE DROP OF THE DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18684063 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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