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[Recalled] ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only. — There have been repor

recall fda device united-states

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
Brand / manufacturerMedline Industries Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0058-2021
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date01 September 2020
EAN / barcode06919010016

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: There have been reports of the suction catheter coming apart from the device assembly during use.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Medline Industries Inc

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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