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[Recalled] CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186 — The filter capacity is not achieved due to damage of the filter membrane | FDA 2019-07-10

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductCE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
Brand / manufacturerB. Braun Medical, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2470-2019
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date10 July 2019
EAN / barcode0061536043

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The filter capacity is not achieved due to damage of the filter membrane.

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 B. Braun Medical, 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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