NA MIC3152Recalls & reported problems
Sterilmed, Inc. · SCISSOR TIP MINI ENDOCUT · 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 10888551001816), received between Oct 4, 2019 and Oct 4, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K073613); they may or may not involve this specific model.
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
- Device Dislodged or Dislocated1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 4, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT A PATIENT UNDERWENT A LAPAROSCOPIC ROUX-EN-Y GASTRIC BYPASS PROCEDURE WITH A REPROCESSED SCISSOR TIP MINI ENDOCUT, AND A PIECE OF THE DEVICE DISLODGED IN THE ABDOMEN OF THE PATIENT. THE PIECE WAS RETRIEVED BY THE SURGEON AND THE PRODUCT WAS REPLACED. THERE WERE NO ISSUES NOTICED PRIOR TO THE DISLODGEMENT AND NO KNOWN CIRCUMSTANCE THAT MAY HAVE CONTRIBUTED. THERE WAS A DELAY TO THE PROCEDURE. HOWEVER, THE PROCEDURE WAS COMPLETED WITH NO PATIENT CONSEQUENCE. MULTIPLE ATTEMPTS HAVE BEEN MADE TO OBTAIN CLARIFICATION TO THIS COMPLAINT AND WHICH PART OF THE DEVICE DISLODGED. HOWEVER, NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9158994 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K073613. One submission often covers many models, so check the product and lot details in each record.
- Z-1846-2016 · Apr 26, 2016 · TerminatedReprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive and open surgical procedures to facilitate cutting, preparatio
- Z-0570-2009 · Aug 8, 2008 · TerminatedScissor Tips Model #'s: AESPO888 AESPO889 ENCES0102 MIC3112 MIC3122 MIC3142 MIC3152 SNO89-5100 and SNO89-5300 Intended to be used with a resusable hand piece and are designed to
Other ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED devices
- Medline LF4418CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed3 recalls8 reports
- Medline LF1937CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls13 reports
- Medline LF1944CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls12 reports
- MEDLINE LF1837CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls4 reports
- Medline LF1844CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed2 recalls1 report
- N/A LF1837Stryker Sustainability Solutions, Inc. · ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED70 reports
- MEDLINE LF1212ACRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed1 recall8 reports
- MEDLINE LF1637CRMedline Industries, Inc. · Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.