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Soft/Soft Spring Clip A1801Recalls & reported problems

Applied Medical Resources Corporation · 3/4 Force Surgical Spring Clip · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00607915110734), received between Jun 23, 2016 and Jun 23, 2016 — classified as 1 malfunction.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • 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.

  • MalfunctionJun 23, 2016Break; Break

    CAGS - "SECURED MAMMARY VESSEL WITH STEALTH A1801, THEN WHILE WORKING ON THE HEART NOTICED EXCESSIVE BLEEDING, WHEN CHECKED CLAMP FOUND IT HAD BROKEN APART. PATIENT IS FINE." TYPE OF INTERVENTION: "THE BLOOD VESSEL HAD TO BE RE-SECURED WITH A SECOND CLAMP." PATIENT STATUS- "FINE."

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 5746977 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.