Reported Oct 16, 2019 · Terminated

CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355

Centurion Medical Products Corporation

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: Centurion Medical Products Corporation · 100 Centurion Way · Williamston, MI · 48895-9086

Is this the product you have?

  • CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355
Lot codes and dates
    • 2018030250
    • 2018072750
    • 2018090450
    • 2018091750
    • 2018122650
    • 2019011050
    • 2019020450
    • 2019031350
    • 2019040150
Amount recalled
181965 total

This recall covers 35 products

The agency filed one notice per product. You are reading one of them; the other 34 are below.

22 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 3, 2020 · Data as of Sep 19, 4:49 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.