FDADecember 18, 2015device

BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter, 5cc (Council Model); Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.

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

The hazard

Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect inflation volume.

What to do

FDA enforcement status: Terminated

Brands named

c r bard

Recall history

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

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