FDAOctober 6, 2014device

Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interventional kyphoplasty or other interventional procedures, to create and monitor pressure In the balloon catheter and pressure In the balloon catheter and to to deflate the balloon catheter

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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