FDA recall record

Medacta Usa GMK Hinge knee prosthesis recall — FDA Z-0275-2016

Incorrect parts: Packages of the GMK Hinge Tibial Augmentation size 4-10 mm have 5 mm screws instead of 10 mm screws.

Class IIclassification
Z-0275-2016official record ID
Nov 25, 2015report date

Recall record at a glance

Official recordZ-0275-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedacta Usa
Report dateNov 25, 2015
Recall initiation dateApr 17, 2015
Quantity4 units (US)
LocationChicago, IL, United States

Official product description

GMK Hinge knee prosthesis; Model Number: 02.09.TA410; Orthopedics and Orthopedic Surgery

Why the product was recalled

Incorrect parts: Packages of the GMK Hinge Tibial Augmentation size 4-10 mm have 5 mm screws instead of 10 mm screws.

Distribution information

Distributed in the states of IL, OH and UT, and the countries of in Austria, Spain, Australia, France and Switzerland.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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