FDAMarch 7, 2018device

Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized.

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

The hazard

The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.

What to do

FDA enforcement status: Terminated

Brands named

sps sterilizationsps

UPCs

164010320170116401032017021640103201703164010320170416401032017051640103201706164010320170716401032017081640103201709164010320171016401032017111640103201712

Recall history

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

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