FDAOctober 6, 2014device

Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to create and maintain, monitor pressure in the balloon catheter - balloon inflation device for angioplasty procedures

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

The hazard

Additional instructions for use due to inability to raise the pressure above 10 atm during inflation phase may result in an incomplete inflation or delay in procedure

What to do

FDA enforcement status: Terminated

Brands named

perouse medicalperouse

Recall history

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

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Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to create and maintain, monitor pressure in the balloon catheter - balloon inflation device for angioplasty procedures — Recall Details · AllClear