PeriCross Epicardial Access Kit PC-1013Recalls & reported problems
CIRCA Scientific, Inc. · Class 2
Data updated Oct 18, 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 10851498007395), received between Mar 16, 2026 and Mar 16, 2026 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Cardiac Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem
THERE WAS A RIGHT VENTRICULAR PERFORATION WITH THE PERICROSS OBTURATOR. PHYSICIAN USED AN AMPLATZER VASCULAR PLUG TO CLOSE THE PERFORATION. PROCEDURE PROCEEDED SUCCESSFULLY GAINING PERICARDIAL ACCESS USING THE PERICROSS DEVICE. PATIENT WAS FINE.
Patient problems: Cardiac Perforation
MAUDE report 24607285 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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