Reported Oct 14, 2020 · Terminated

ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended…

Medline Industries Inc.

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: Medline Industries Inc · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

    • ClearPro Closed Suction Catheter
    • Model DYNCPDS14T
    • 14 Fr
  • FOR ENDOTRACHEAL TUBE - Product UsageCatheters are intended for endotracheal suction of adult patients with artificial airways. Single use only
Lot codes and dates
  • Model
    • DYNCPDS14T
    • Lots 06919010016 and 06919020016
Amount recalled
6225 units

This recall covers 10 products

The agency filed one notice per product. You are reading one of them; the other 9 are below.

Why it was recalled

There have been reports of the suction catheter coming apart from the device assembly during use.

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 May 27, 2022 · Data as of Sep 19, 6:20 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.