AVANOS 43059Recalls & reported problems
Avanos Medical, Inc. · ON-Q Pain Relief System QUIKBLOC* Over-the-Needle Catheter Set, Stimulating · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00193494430597), received between Jun 24, 2021 and Dec 22, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Material Integrity Problem1
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.
MalfunctionDec 22, 2022Material Integrity Problem; Material Integrity Problem
IT WAS REPORTED, THE CATHETER WENT IN WITH NO PROBLEM, WHEN THEY ATTEMPTED TO REMOVE THE NEEDLE PART IT BROKE AT THE HUB; A HEMOSTAT WAS USED TO REMOVE THE NEEDLE; THE PATIENT WAS NOT HARMED, THE ONQ WAS PLACED.
Patient problems: Foreign Body In Patient
MAUDE report 16037870 ↗MalfunctionJun 24, 2021Break; Break
PROCEDURE: POPLITEAL BLOCK AND THE OTHER AN ADDUCTOR. CATHPLACE: UNKNOWN. IT WAS REPORTED, ONE OF THE TWO CATHETERS WAS MISSING THE BLACK MARKER AT THE CATHETER TIP AND THE MARKER BEFORE THE FIRST HOLE. THE ANESTHESIOLOGIST BELIEVES THAT THE CATHETER WAS NOT BROKEN, BUT IS INTACT. HE THINKS IT WAS MISSING THE BLACK COLORING ON THE TIP, AS WELL AS A COUPLE OF THE INCREMENT MARKERS. THE PATIENT SENT THE PHOTO TO THE NURSE, WHO SHOWED THE PHYSICIAN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12062091 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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