Versaport 179094Recalls & reported problems
Covidien LP · V2 Bladed Trocar · Class 2
All models of Versaport (21)
Data updated Oct 16, 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 20884521081267), received between Jun 19, 2017 and Jun 19, 2017 — classified as 1 malfunction.
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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 19, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO REPORTER DURING THE LAPAROSCOPIC CHOLECYSTECTOMY, THE INSTRUMENT NOT CLOSE THE JAW CLIPS AND BLOCKS THE SAME WITHOUT CLOSING THE CLIP. THERE WAS THERE ANY UNANTICIPATED TISSUE LOSS OR DAMAGE AS A RESULT OF THIS PROBLEM. THERE WAS NO BLOOD LOSS OF 500CC OR MORE DUE TO THE PRODUCT PROBLEM. SURGICAL TIME WAS NOT EXTENDED BY MORE THAN 30 MINUTES DUE TO THE PRODUCT PROBLEM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6650059 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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