FDAAugust 7, 2017device

Spectranetics Bridge Occlusion Balloon catheter, Sheath Compatibility 12F, Guidewire Compatibility 0.035in, Working Length 90cm, Balloon Outer Diameter 31mm, Balloon Length 80mm, Rx Only. Product Usage: It is a device used to occlude the vessel and prevent blood loss as the physician preps for su...

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

The hazard

Possible inability to pass the guidewire through the Bridge device, therefore, resulting in a potential delay of treatment.

What to do

FDA enforcement status: Terminated

Brands named

spectranetics

Recall history

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

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