NA 0250080267Recalls & reported problems
Stryker Corporation · Insert, Endo Metzenbaum Scissors (Curved) · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327052756), received between Oct 18, 2018 and May 22, 2023 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Break” (2 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.
Most reported problems
Device problems
- Break2
- Arcing1
- Temperature Problem1
Patient problems
- No Known Impact Or Consequence To Patient2
- Burn(s)1
- Superficial (First Degree) Burn1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2023Arcing; Temperature Problem; Arcing; Temperature Problem
IT WAS REPORTED THAT THE PATIENT WAS BURNED.
Patient problems: Burn(s); Superficial (First Degree) Burn
MAUDE report 16981364 ↗InjuryJul 10, 2019Break
IT WAS REPORTED THAT THE TIP BROKE AND POTENTIALLY REMAINED INSIDE THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8776193 ↗InjuryOct 18, 2018Break
IT WAS REPORTED THAT THE TIP OF THE SCISSORS BROKE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7981117 ↗
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- Single Use Retrieval Basket V FG-V432POlympus Medical Systems Corp. · Endoscopic grasping/cutting instrument, non-powered11 reports
- n.a. 27072AKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered9 reports
- n.a. 27074BKarl 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 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.
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