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FDAJanuary 13, 2020device

Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

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

The hazard

There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

Recall history

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

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