Recall of Blood Component Infusion Set

infusion recall

Recall – Incorrectly Labeled Filter

The Food and Drug Administration (FDA), along with Fenwal, Inc of Illinois, has announced a recall of their Blood Component Infusion Set, as Fenwal has identified a labeling issue with Product 4C2223.

It has been determined that the package label for the Blood Component Infusion Set incorrectly states 80 Micron filter, when the actual filter size is a standard blood filter of 170-260 micron in size.

Fenwal is recommending that customers immediately discontinue the use of this product and return the product to Fenwal.

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