ZIPCLIP 529500001061Recalls & reported problems
Synovis Micro Companies Alliance, Inc · Automatic Microclip Applier · Class 2 · Implant
- 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 00844735006384), received between Sep 25, 2025 and Sep 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (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.
Reports received per month
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2025Unintended Movement; Unintended Movement
IT WAS REPORTED THAT DURING USE OF AN AUTOMATIC MICROCLIP APPLIER (ZIPCLIP), A CLIP ROTATION ISSUE OCCURRED. THE MICROCLIP WAS APPLIED TO THE VESSEL WITH NO ISSUES. WHEN THE DEVICE JAWS OPENED, THE NEXT CLIP LOADED SIDEWAYS IN THE JAW. THE SURGEON OBSERVED THIS AND PASSED THE DEVICE TO SURGICAL TECH. A NEW ZIPCLIP DEVICE WAS PASSED TO THE SURGEON AND THE CASE CONTINUED. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23151497 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.