FDAJune 10, 2021device

basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or other interventional device, and to measure the pressure within the balloon.

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

The hazard

Due to a design issue, inflation syringe handle separating from the inflation device when handle is withdrawn.

What to do

FDA enforcement status: Terminated

Brands named

merit medical systemsmeritmerit medical

UPCs

0088445044017900884450510155008844505112200088445051130500884450511510

Recall history

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

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