NA 0295727200Recalls & reported problems
Stryker Corporation · Hip Bridge, Dual Rotating Stopcocks · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327053074), received between Dec 9, 2021 and Jul 16, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Component Missing” (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.
Reports received per month
Most reported problems
Device problems
- Component Missing2
- Insufficient Device Problem Information2
- Contamination /Decontamination Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 16, 2025Component Missing; Insufficient Device Problem Information; Component Missing; Insufficient Device Problem Information
IT WAS REPORTED THAT THE TRAY WAS BEING USED ON THE OPERATING FIELD. IT TURNS OUT THAT IT WAS NOT FUNCTIONAL. THE PATIENT WAS PUT TO SLEEP AND AWAKENED ON THE TABLE, WITH NO SURGERY POSSIBLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22524452 ↗MalfunctionJul 15, 2025Component Missing; Insufficient Device Problem Information; Component Missing; Insufficient Device Problem Information
IT WAS REPORTED THAT THE TRAY WAS BEING USED ON THE OPERATING FIELD. IT TURNS OUT THAT IT WAS NOT FUNCTIONAL. THE PATIENT WAS PUT TO SLEEP AND AWAKENED ON THE TABLE, WITH NO SURGERY POSSIBLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22515955 ↗MalfunctionDec 9, 2021Contamination /Decontamination Problem
IT WAS REPORTED THAT THERE WAS FOREIGN MATERIAL.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 12968516 ↗
Other Accessories, arthroscopic devices
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- NA 228302Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC287 reports
- FIRSTPASS 72290128Smith & Nephew, Inc. · ACCESSORIES,ARTHROSCOPIC232 reports
- NA 251723Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC145 reports
- COBRA 3910900093Stryker Corporation · Accessories, arthroscopic138 reports
- FirstPass 72290129Smith & Nephew, Inc. · Accessories, arthroscopic82 reports
- FirstPass 72290130Smith & Nephew, Inc. · Accessories, arthroscopic80 reports
- MITEK 242025Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC61 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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