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Halyard 13618Recalls & reported problems

Avanos Medical, Inc. · HALYARD* ON-Q* Pump Kits With ON-Q* SILVERSOAKER* Catheter · Class 2

All models of Halyard (232)

Data updated Oct 18, 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 10680651136180), received between Jul 19, 2019 and Jul 19, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K063530); they may or may not involve this specific model.

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.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 19, 2019Break; Break

    FILL VOLUME: 270 ML. FLOW RATE: 4 ML/HR. PROCEDURE: PARTIAL MASTECTOMY LEFT BREAST. CATHPLACE: DUAL PLACEMENT LEFT AXILLA/LEFT BREAST. INFUSION START TIME: UNKNOWN. INFUSION STOP TIME: UNKNOWN. IT WAS REPORTED THAT THE PATIENT UNDERWENT A PARTIAL MASTECTOMY LEFT BREAST ON (B)(6) 2019. DURING THE FOLLOW-UP VISIT ON (B)(6) 2019 WHERE CATHETERS WERE BEING REMOVED, CATHETER TIP OF THE AXILLA PLACED CATHETER BROKE OFF. SURGICAL EXPLORATION OF THE INCISION SITE & CATHETER TRACT WAS PERFORMED ON (B)(6) 2019; TIP WAS NOT RECOVERED. NO PATIENT ADVERSE EFFECTS OR PATIENT INJURY REPORTED. NO REPORTED ISSUES WITH THE PUMP; PUMP FUNCTIONED WITHOUT INCIDENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8809108 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K063530. One submission often covers many models, so check the product and lot details in each record.

  • Z-2860-2011 · Apr 15, 2011 · Terminated
    I-Flow ON-Q with Select-A-Flow Pumps, Intended for continuous and/or intermittent delivery of medication to and around surgical wound sites and/or close proximity to nerves for p
  • Z-2133-2008 · Feb 14, 2008 · Terminated
    On-Q C-bloc 400 ml, 1-7 ml/hr Select-A-Flow + 5 ml/60 min ONDEMAND, REF CB005 indicated for continuous and/or intermittent delivery of medication (such as local anesthetics or narc
  • Z-1869-2008 · Feb 12, 2008 · Terminated
    ON-Q PainBuster Infusion Pump (270 ml, 5 ml/hr), REF PS6504, Part No. 5001260. The pump is indicated for continuous and/or intermittent delivery of medication (such as local anest

Other PUMP, INFUSION, ELASTOMERIC devices

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Sources and updates

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