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FDAAugust 10, 2023device

Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular

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

The hazard

This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

What to do

FDA enforcement status: Ongoing

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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Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular — Recall Details · AllClear