Cope G04474Recalls & reported problems
Cook Incorporated · Cope Gastrointestinal Suture Anchor Set · Class 2 · Implant
All models of Cope (23)
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 00827002044746), received between Apr 28, 2016 and Apr 28, 2016 — classified as 1 injury.
The most frequently reported specific device problem is “Material Separation” (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
- Material Separation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 28, 2016Material Separation; Material Separation
DURING A PERCUTANEOUS GASTROSTOMY PROCEDURE, THE ANCHOR OF GIAS-100 DETACHED WHEN THE DOCTOR APPLIED TRACTION TO THE SUTURE, IN ORDER TO PULL THE STOMACH WALL CLOSE TO THE ABDOMINAL WALL. THEY ARE WAITING FOR THE ANCHOR TO PASS VIA THE GI SYSTEM. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: Foreign Body In Patient
MAUDE report 5615603 ↗
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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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