FDAMarch 11, 2025device

BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118, CK000955, 3174135, CK000617, CK000839, 3194355, 6174118, 3194135, 3194335, 2174108, 9194118, 3194118, 1174118, CK000285C, CK000335A, CK000796, 1194108D, CK000757, CK001042, 91...

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

The hazard

Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.

What to do

FDA enforcement status: Ongoing

Brands named

bard access systemsbardbard access

UPCs

008017410276110080174110514200801741027598008017410993970080174102762800801741027635008017410288470080174103556200801741200922008017410276040080174112228600801741154393

Recall history

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

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