Reported Oct 3, 2012 · Terminated

Catheter Irrigation Set labeled in part: ***24K Arthroscopy Outflow/Suction Tubing Set*** This Arthroscopy Tubing Set…

Linvatec Corp. dba ConMed Linvatec

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Linvatec Corp. dba ConMed Linvatec · 11311 Concept Blvd · Largo, FL · 33773-4908

Is this the product you have?

  • Catheter Irrigation Set labeled in part***24K Arthroscopy Outflow/Suction Tubing Set*** This Arthroscopy Tubing Set is intended for use, in conjunction with the ConMed Linvatec 24k Pump, for pump-induced outflow and/or suction of fluid from the joint during arthroscopic procedures
Lot codes and dates
  • Catalog # 24k100 Lot #:
    • 20853-000
    • 20854-000
    • 20855-000
    • 21791-000
    • 22172-000
    • 22414-000
    • 22513-000
    • 22667-000
    • 22724-000
    • 22725-000
    • 23606-000
    • 23912
    • 23912-000
    • 23971-000
    • 24177-000
    • 24296-000
    • 24348-000
    • 24373-000
    • 24476-000
    • 24559-000
    • 24671-000
    • 24703-000
    • 24905-000
    • 25668-000
    • 25794-000
    • 25931-000
    • 26025-000
    • 26041-000
    • 26294-000
    • 26448-000
    • 26486-000
    • 27130-000
    • 27255
    • 27255-000
    • 27322
    • 27520
Amount recalled
30064 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

ConMed Linvatec recalled their 24k Arthroscopy Outflow/Suction Tubing Set (Product Number 24k100)because there is a possibility that the product may have a breach in the Tyvek seal that could potentially compromise the sterility of the contents.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 25, 2013 · Data as of Sep 19, 5:25 PM UTC

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