Skip to content

Performer G10387Recalls & reported problems

Cook Incorporated · Check-Flo Performer Introducer Set Micropuncture, Radial Artery Access · Class 2

All models of Performer (62)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00827002103870), received between Jul 15, 2022 and Jul 15, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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

  • Contamination /Decontamination Problem1

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.

  • MalfunctionJul 15, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED, UPON OPENING A PERFORMER RADIAL ACCESS SET'S STERILE PACKAGING, A STAIN/FOREIGN MATTER WAS PRESENT ON THE PRODUCT. THE DEVICE WAS NOT USED AND THERE WERE NO CONSEQUENCES FOR THE PATIENT. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15027705 ↗

Other INTRODUCER, CATHETER devices

All INTRODUCER, CATHETER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page