Reported Mar 11, 2015 · Terminated

Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100,…

Baxter Corporation Englewood

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 Corporation Englewood · 14445 Grasslands Dr · Englewood, CO · 80112-7062

Is this the product you have?

  • Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.
Lot codes and dates
  • All DiscPac products are affected within expiry up to October 2017
Amount recalled
1,404,230

Where it was sold

  • Nationwide

Why it was recalled

Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.

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 Aug 8, 2016 · Data as of Sep 19, 6:17 PM UTC

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