FDADecember 28, 2017device

PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray with Tyvek lid within a header bag configuration or a breather bag configuration.

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

The hazard

Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC catheters at the luer hub extension leg junction.

What to do

FDA enforcement status: Terminated

Brands named

bard access systemsbardbard access

Recall history

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

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