VUETIP VUETIP10Recalls & reported problems
Conmed Corporation · VueTip Trocar Swab Accessory Kit Laparoscopic Solutions · Class 2
- 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 20845854061777), received between Oct 12, 2023 and Oct 12, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Fell” (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.
Reports received per month
Most reported problems
Device problems
- Device Fell1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 12, 2023Device Fell; Device Fell
THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER, THAT THE VUETIP10, VUETIP STERIL TROCAR CLEAN KIT WAS BEING USED DURING A ROBOTIC PROCEDURE ON (B)(6) 2023 DATE WHEN IT WAS REPORTED ¿THE CLEANING STICK (VUETIP) WAS INSERTED INTO THE ABDOMEN VIA A ROBOTIC PORT. THIS IS IN SUCH A WAY THAT THEY HAVE CLEANED THE ROBOT PORT, THEY HAVE LEFT THE CLEANING STICK BEHIND AND AT THE SAME TIME USED THE SUCTION IN THE ABDOMEN. THIS HAS THEN CAUSED THE CLEANING STICK TO BE SUCKED INTO THE ABDOMEN ON THE BASIS OF A NEGATIVE PRESSURE. THEY HAVE BEEN USED TO THE FACT THAT THERE IS A STOP IN THE BACK PART OF THE CLEANING STICK THAT HAS PREVENTED THIS.THE VUETIP CAN BE BENT AT THE REAR END TO PREVENT THIS, BUT THE STICK WILL THEN BE SLIGHTLY SHORTER, BUT IS SUFFICIENT FOR CLEANING BOTH STANDARD TROCARS AND ROBOTIC PORTS. IT IS OF COURSE A DIFFERENT HANDLING AND THERE IS A LIMITATION THAT THE VUETIP DOES NOT HAVE A STOP AT THE BACK OF THE STICK. NO DAMAGE OCCURRED AS THE PRODUCT IS FOUND AND CAN BE TAKEN OUT OF THE SAME PORT." THE PROCEDURE WAS COMPLETED WITH THE USE OF AN ALTERNATE PEANG WITH STERILE COMPRESS DEVICE AND A 10-MINUTE DELAY WAS ALSO REPORTED. THERE WAS NO REPORT OF INJURY, ME
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17919462 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.