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InterValve Recalls

1 recall on record · May 21, 2014 to May 21, 2014 · Medical Devices

May 21, 2014Medical DevicesFDA

InterValve Inc recalls InterValve V8 Balloon Aortic Valvuloplasty Catheter, model 172212C110, 192412C110, 212612C110, 232812C110. Used in Car

Hazard: Leak issues were discovered through accelerated age testing.

InterValve Recalls | RecallWatchUSA