Reported May 15, 2013 · Terminated

A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set, 5.7", Vol. 0.8 mL, 2 Injection Sites, Male Luer Lock…

Baxter Healthcare Corp.

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: Baxter Healthcare Corp. · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • A) Product Code 2N3371
    • Non-DEHP Y-Type Catheter Extension Set
    • 5.7"
    • Vol. 0.8 mL
    • 2 Injection Sites
    • Male Luer Lock Adapter
  • Single use only Product UsageThis device is indicated for use in blood sampling and the administration of solutions. The InterLink Injection Site feature is intended to eliminate accidental needle sticks when used in conjunction with an InterLink Cannula as part of an I.V. needless access system
Lot codes and dates
  • A) Product Code 2N3371
    • Lots R12H23076
    • R12H30097
    • R12I0707
    • R12I08059
    • R12I25046
    • R12I2607
    • R12J11052
    • R12J12068
    • R12J13058R12K17057
    • R12L10084
    • R13A12057
Amount recalled
A) Product Code 2N3371: 228,200 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Customers have reported that when separating an individual package from its attached grouping, the adjacent package has opened, compromising its sterile barrier properties.

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 31, 2017 · Data as of Sep 19, 6:17 PM UTC

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