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Medacta Usa Inc recalls Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty
Recalled October 31, 2018 · FDA recall Z-0196-2019 · Medacta Usa
Hazard
Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem. · FDA Class II
Units
837 units
Sold at
NC, ID, Belgium, Switzerland, Spain, Germany, Australia, France, Italy
Description
Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem.
Product
Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.
Manufacturer(s)
Medacta Usa Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →