FDAMarch 13, 2019device

Procedure kits include devices from the affected lots distributed OUS only: (1)BOX KIT00529H KIT COLECISTECTOMIA ACCESO (2)BOX KIT00680 KIT COLECISTECTOMIA- (3)BOX KIT00681 KIT APENDICECTOMIA (4)BOX KIT00897 KIT COLON IZQUIERDO (5)BOX LAPL1 ZESTAW DO CHOLECYSTEKTOMII (6)BOX PST01134 LAP CHOLE KIT...

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

The hazard

Sterilization method used was not consistent with the labeling and the approved sterilization method

What to do

FDA enforcement status: Terminated

Brands named

covidien

Recall history

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

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