Skip to content

AVANOS 43056Recalls & reported problems

Avanos Medical, Inc. · ON-Q Pain Relief System QUIKBLOC* Over-the-Needle Catheter Set · 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 00193494430566), received between Jul 20, 2020 and Jul 20, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1

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.

  • MalfunctionJul 20, 2020Fracture; Fracture

    IT WAS REPORTED THE PATIENT'S RIGHT SIDED RECTUS SHEATH BECAME STUCK. REMOVAL OF THE CATHETER WAS ATTEMPTED BY THE TEAM CONSULTANT DOCTOR. THE CATHETER WAS REMOVED, BUT WAS MISSING THE BLUE TIP. THE PATIENT WAS INSTRUCTED TO HAVE AN MRI (MAGNETIC RESONANCE IMAGING) OR CT (COMPUTED TOMOGRAPHY) SCAN AS AN OUTPATIENT TO CONFIRM THE POSITION OF THE TIP, AND, IF REMOVAL IS NECESSARY, THEN IT WILL BE REMOVED UNDER LOCAL ANESTHETIC.

    Patient problems: Foreign Body In Patient

    MAUDE report 10298826 ↗

Other CATHETER, CONDUCTION, ANESTHETIC devices

All CATHETER, CONDUCTION, ANESTHETIC devices →

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