Thoracoport 179310Recalls & reported problems
Covidien LP · Soft Trocar · Class 2
All models of Thoracoport (7)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 20884521081236), received between Feb 21, 2025 and Feb 21, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (5 reports).
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.
Reports received per month
Most reported problems
Device problems
- Break5
- Product Quality Problem5
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 21, 2025Break; Product Quality Problem; Break; Product Quality Problem
ACCORDING TO THE REPORTER, PRIOR TO USE, THE OBTURATOR/TROCAR BROKE. ADDITIONALLY, CLEAR LIQUID WAS ADHERED TO THE CANNULA PORTION OF THE 5 TROCARS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21439409 ↗MalfunctionFeb 21, 2025Break; Product Quality Problem; Break; Product Quality Problem
ACCORDING TO THE REPORTER, PRIOR TO USE, THE OBTURATOR OR TROCAR BROKE. ADDITIONALLY, CLEAR LIQUID WAS ADHERED TO THE CANNULA PORTION OF THE FIVE TROCARS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21439262 ↗MalfunctionFeb 21, 2025Break; Product Quality Problem; Break; Product Quality Problem
ACCORDING TO THE REPORTER, PRIOR TO USE, THE OBTURATOR OR TROCAR BROKE. ADDITIONALLY, CLEAR LIQUID WAS ADHERED TO THE CANNULA PORTION OF THE FIVE TROCARS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21439228 ↗MalfunctionFeb 21, 2025Break; Product Quality Problem; Break; Product Quality Problem
ACCORDING TO THE REPORTER, PRIOR TO USE, THE OBTURATOR OR TROCAR BROKE. ADDITIONALLY, CLEAR LIQUID WAS ADHERED TO THE CANNULA PORTION OF THE FIVE TROCARS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21438805 ↗MalfunctionFeb 21, 2025Break; Product Quality Problem; Break; Product Quality Problem
ACCORDING TO THE REPORTER, PRIOR TO USE, THE OBTURATOR OR TROCAR BROKE. ADDITIONALLY, CLEAR LIQUID WAS ADHERED TO THE CANNULA PORTION OF THE FIVE TROCARS. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21437719 ↗
Other Laparoscope, general & plastic surgery devices
- HIGH DEFINITION LCD MONITOR OEV262HOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,937 reports
- HD AUTOCLAVABLE CAMERA HEAD OTV-S7ProH-HD-12EOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,886 reports
- HD AUTOCLAVABLE CAMERA HEAD OTV-S7ProH-HD-10EOlympus Medical Systems Corp. · Laparoscope, general & plastic surgery1,086 reports
- Auto Suture OMS-T10BTCovidien LP · Laparoscope, general & plastic surgery1 recall955 reports
- PDB OMS-PDB1000Covidien LP · Laparoscope, general & plastic surgery859 reports
- VISERA 4K UHD CAMERA CONTROL UNIT OLYMPUS OTV-S400Olympus Medical Systems Corp. · Laparoscope, general & plastic surgery777 reports
- Auto Suture OMS-T10SBCovidien LP · Laparoscope, general & plastic surgery1 recall697 reports
- Spacemaker SMBTTRNDXCovidien LP · Laparoscope, general & plastic surgery590 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 · 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.
How reports and recalls are matched · Editorial policy · Report an error on this page