COBRA 3910900092Recalls & reported problems
Stryker Corporation · COBRA SUTURE PASSER, HOOK · Class 1
All models of COBRA (2)
Data updated Oct 18, 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 07613327413588), received between Sep 22, 2023 and Jan 24, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (3 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Material Twisted/Bent3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 24, 2024Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE NEEDLE BECAME BENT WHILE THE DEVICE WAS IN USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18576490 ↗MalfunctionOct 19, 2023Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE NEEDLE BECAME BENT WHILE THE DEVICE WAS IN USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17967600 ↗MalfunctionSep 22, 2023Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE NEEDLE BECAME BENT WHILE THE DEVICE WAS IN USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17801806 ↗
Other Accessories, arthroscopic devices
- Arthrex® AR-12990Arthrex, Inc. · Accessories, arthroscopic409 reports
- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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