AVANOS 43057Recalls & reported problems
Avanos Medical, Inc. · ON-Q Pain Relief System QUIKBLOC* Over-the-Needle Catheter Set, Stimulating · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00193494430573), received between Nov 23, 2021 and Apr 6, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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
- Break2
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2023Break; Break
IT WAS REPORTED, THE QUICKBLOC NEEDLE AND CATHETER WERE SUCCESSFULLY PLACED; WHEN THE CERTIFIED REGISTERED NURSE ANESTHETIST (CRNA) STUDENT ATTEMPTED TO REMOVE THE NEEDLE FROM THE CATHETER, AND THEY REALIZED THE CATHETER WAS STUCK. THE CRNA USED HEMOSTATS TO SEPARATE THE NEEDLE AND CATHETER AND REALIZED THE HUB AND CATHETER HUB WERE BROKEN APART LEAVING THE CATHETER INSIDE THE PATIENT. THERE WAS NO REPORTED INJURY OR MEDICAL INTERVENTION.
Patient problems: Foreign Body In Patient
MAUDE report 16689086 ↗MalfunctionNov 23, 2021Break; Break
IT WAS REPORTED THE NEEDLE BROKE "WHILE ANESTHESIA WAS PERFORMING AN ADDUCTOR CANAL BLOCK FOR A TOTAL KNEE REPLACEMENT PROCEDURE." THE REPORTED PRODUCT WAS REMOVED FROM THE PATIENT AND A NEW PRODUCT WAS USED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12865227 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.