Vyaire V-178501Recalls & reported problems
Jaeger Medical GmbH · Vyntus WALK · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 54250892904899), received between Apr 17, 2024 and Apr 3, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Battery Problem” (4 reports).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Battery Problem4
- Failure to Calibrate1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 3, 2025Battery Problem; Battery Problem
THE CUSTOMER COMPLAINED THAT THE BATTERY OF THE VYNTUS WALK TABLET IS SWOLLEN. THERE WAS NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21761616 ↗MalfunctionApr 3, 2025Battery Problem; Battery Problem
THE CUSTOMER COMPLAINED THAT THE BATTERY OF THE VYNTUS WALK TABLET IS SWOLLEN. THERE WAS NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21761606 ↗MalfunctionJun 18, 2024Battery Problem; Battery Problem
INITIALLY IT WAS REPORTED BY THE CUSTOMER THAT THE TABLET DOES NOT WORK. THE SCREENS ARE SEPARATING AND IT DOES NOT POWER UP. THE DEVICE WAS RETURNED FOR AN INVESTIGATION. ON 29-MAY-2024 IT WAS FOUND, THAT THE BATTERY OF THE DEVICE IS SWOLLEN. THE AWARENESS DATE WILL BE CHANGED TO THE 29-MAY-2024, BECAUSE THE INITIAL DESCRIPTION OF THE FAILURE DID NOT INDICATE A REPORTABLE EVENT. THERE WAS NO PATIENT INVOLVEMENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19557722 ↗MalfunctionJun 13, 2024Battery Problem; Battery Problem
THE CUSTOMER COMPLAINED THAT THE BATTERY OF THE VYNTUS WALK TABLET IS SWOLLEN. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19526927 ↗MalfunctionApr 17, 2024Failure to Calibrate; Failure to Calibrate
THE CUSTOMER COMPLAINED THAT THE BATTERY OF THE LENOVO TABLET IS SWOLLEN. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19123956 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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