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[Recalled] Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992207 Version A, Sterile EO, Rx Only — There is a potential that valve assemblies will not open | FDA 2023-04-22

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductAspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992207 Version A, Sterile EO, Rx Only
Brand / manufacturerMerit Medical Systems, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1909-2023
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date22 April 2023
EAN / barcode00884450398166

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: There is a potential that valve assemblies will not open. preventing fluid from draining.

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 Merit Medical Systems, 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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