FDADecember 20, 2019device

Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Product lidstock contains the incorrect expiration date for the product

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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