Mini Port 171315Recalls & reported problems
Covidien LP · Introducer · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521066301), received between May 18, 2020 and Aug 30, 2021 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
- Detachment of Device or Device Component1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 30, 2021Break; Break
ACCORDING TO THE REPORTER, DURING A PEDIATRIC SURGERY INGUINAL HERNIA SURGERY, THE DEVICE HAD A DAMAGED NEEDLE TIP. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12384151 ↗InjuryMay 18, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, DURING A THORACO WEDGE SEGMENTAL RESECTION, THERE WAS A WHITE PLASTIC FRAGMENT IN THE CHEST CAVITY WHEN THE CHEST WAS CLOSED USING THE DEVICE, AND THE FRAGMENT COULD NOT BE RETRIEVED.
Patient problems: Foreign Body In Patient
MAUDE report 10064942 ↗
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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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