Portrait VSM MVC101Recalls & reported problems
Ge Medical Systems Information Technologies, Inc. · Portrait VSM ATO MODEL · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Sep 26, 2025Class IIOpen, Classified
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Z-0456-2026 · Root cause: Component change control · Recall details · FDA record ↗
Other Oximeter, ear devices
- MasimoSET LNCS® TC-I SpO2 Reusable Ear Sensor 1895Masimo Corporation · Oximeter, ear1 recall3 reports
- MasimoSET® M-LNCS™ TC-I SpO2 Reusable Ear Sensor 2503Masimo Corporation · Oximeter, ear1 recall1 report
- TruSignal SpO2 TS-SE-3GE Healthcare Finland Oy · Oximeter, ear1 recall0 reports
- V-Sign™ Sensor 2 VS-A/P/NSenTec AG · Oximeter, Ear1 recall0 reports
- MasimoSET® LNOP® TC-I SpO2 Reusable Ear Sensor 1794Masimo Corporation · Oximeter, ear1 recall0 reports
- Membrane Changer (single-use) / single unit MCSenTec AG · Oximeter, Ear1 recall0 reports
- TruSignal SpO2 TS-APGE Healthcare Finland Oy · Oximeter, ear1 recall0 reports
- TruSignal SpO2 TS-W-DGE Healthcare Finland Oy · Oximeter, ear1 recall0 reports
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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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