NA 0250080265Recalls & reported problems
Stryker Corporation · Insert, Curved Metzenbaum Scissors (Long Jaws) · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327052633), received between Aug 7, 2018 and Feb 5, 2025 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Break” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break4
- Material Fragmentation2
- Detachment of Device or Device Component1
- Device Fell1
Patient problems
- No Known Impact Or Consequence To Patient3
- No Clinical Signs, Symptoms or Conditions2
- Foreign Body In Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2025Break; Material Fragmentation; Break; Material Fragmentation
IT WAS REPORTED THAT THE DEVICE BROKE DURING PROCEDURE. THE BROKEN PIECE(S) WERE SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21316006 ↗InjuryJul 31, 2024Break; Material Fragmentation; Break; Material Fragmentation
IT WAS REPORTED THAT THE DEVICE BROKE AND POTENTIALLY REMAINED IN THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19878723 ↗MalfunctionDec 16, 2019Break
IT WAS REPORTED THAT THE TIP OF THE SCISSOR BROKE OFF. THE BROKEN PIECES WERE RETRIEVED.
Patient problems: Foreign Body In Patient; No Known Impact Or Consequence To Patient
MAUDE report 9474606 ↗InjuryAug 21, 2018Detachment of Device or Device Component; Device Fell
IT WAS REPORTED THAT A PIECE OF THE SCISSOR FELL OFF DURING A CASE. ADDITIONAL INFORMATION RECEIVED STATES IT WAS NOT KNOWN IF THE BROKEN PIECE WAS RETRIEVED FROM THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7802398 ↗MalfunctionAug 7, 2018Break
IT WAS REPORTED THAT THE TIP BROKE DURING A PROCEDURE. THE TIP WAS RETRIEVED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7760111 ↗
Other Endoscopic grasping/cutting instrument, non-powered devices
- diagnostic FTRD Set 13Ovesco Endoscopy AG · Endoscopic Grasping/Cutting Instrument, Non-Powered13 reports
- Single Use Retrieval Basket V FG-V422PROlympus Medical Systems Corp. · Endoscopic grasping/cutting instrument, non-powered1 death11 reports
- Single Use Retrieval Basket V FG-V432POlympus Medical Systems Corp. · Endoscopic grasping/cutting instrument, non-powered11 reports
- n.a. 27074BKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered9 reports
- n.a. 27072AKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered9 reports
- Raptor 00711177US Endoscopy · Endoscopic grasping/cutting instrument, non-powered8 reports
- n.a. 27071TJKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered6 reports
- Raptor 00711178US Endoscopy · Endoscopic grasping/cutting instrument, non-powered5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.