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N/A (REF 5DCD)Recalls & reported problems

Stryker Sustainability Solutions, Inc. · Endopath Curved Dissector w/Unipolar Cautery · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885825013301), received between Aug 30, 2017 and Aug 30, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • 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.

  • InjuryAug 30, 2017Break; Break

    IT WAS REPORTED THAT THE TIP OF THE LAPAROSCOPIC INSTRUMENT BROKE OFF DURING THE OPERATION AND HAD TO BE RETRIEVED. THE PIECE WAS RETRIEVED USING FLUOROSCOPY AND A GRASPER. THE PATIENT WAS NOT OPENED UP. THE SURGICAL DELAY WAS APPROXIMATELY 1.5 ¿ 2 HOURS LOCATING THE BROKEN PIECE. THERE WAS NO PATIENT INJURY REPORTED. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

    MAUDE report 6833089 ↗

Other ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED devices

All ELECTROSURGICAL, CUTTING & COAGULATION ACCESSORIES, LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED devices →

Sources and updates

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