FDAMay 17, 2021device

Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715

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

The hazard

The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.

What to do

FDA enforcement status: Terminated

Brands named

adria srladria

Recall history

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

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