Versaport 177794Recalls & reported problems
Covidien LP · Reusable Cannula · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521078475), received between Nov 16, 2018 and Nov 16, 2018 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Foreign Body In Patient1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 16, 2018Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, AFTER A LAPAROSCOPIC OOPHOROCYSTECTOMY THE BREAKAGE OF THE TROCAR TIP WAS CONFIRMED. BECAUSE IT WAS POSTOPERATIVE, THE SECOND PROCEDURE WAS PERFORMED. DURING THE SECOND PROCEDURE, THE PATIENT¿S CAVITY WAS OBSERVED, BUT NO FRAGMENTS WERE FOUND. THE FRAGMENTS FOUND IN THE OPERATION ROOM FITTED THE DAMAGED PART, BUT THE SIZE DID NOT MATCH. THE PART FELL INTO THE PATIENT'S CAVITY AND COULD NOT BE RETRIEVED.
Patient problems: Foreign Body In Patient; No Code Available
MAUDE report 8077792 ↗
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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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