FDA recall record

Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total recall — FDA Z-0196-2019

Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem.

Class IIclassification
Z-0196-2019official record ID
Oct 31, 2018report date

Recall record at a glance

Official recordZ-0196-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedacta Usa Inc.
Report dateOct 31, 2018
Recall initiation dateNov 15, 2017
Quantity837 units
LocationMemphis, TN, United States

Official product description

Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.

Why the product was recalled

Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem.

Distribution information

NC, ID, Belgium, Switzerland, Spain, Germany, Australia, France, Italy

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: Telephone.

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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