VidiaPortRecalls & reported problems across all models
Baxter Medical Systems GmbH + Co. KG · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one VidiaPort model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 3 models of VidiaPort by Baxter Medical Systems GmbH + Co. KG in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Nov 13, 2024 and Nov 13, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
VidiaPort recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jun 4, 2024Open, Classified
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads
Z-2313-2024 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗
Most reported VidiaPort problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
VidiaPort models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- VidiaPort 4028110CAMERA, SURGICAL AND ACCESSORIES1 recall1 report
- VidiaPort 4028310CAMERA, SURGICAL AND ACCESSORIES1 recall0 reports
- VidiaPort 4028210CAMERA, SURGICAL AND ACCESSORIES1 recall0 reports
Recent VidiaPort adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionNov 13, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
CUSTOMER REPORTED THE SPRING ARM DETACHED FROM THE CENTRAL AXIS BUT DID NOT FALL DOWN. NO HARM OR SIGNIFICANT IMPACT TO THE PROCEDURE WAS REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20673913 ↗
Other Baxter Medical Systems GmbH + Co. KG products
All Baxter Medical Systems GmbH + Co. KG devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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