Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.
Reported: October 31, 2018 Initiated: November 15, 2017 #Z-0196-2019
Product Description
Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.
Reason for Recall
Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem.
Details
- Recalling Firm
- Medacta Usa Inc
- Units Affected
- 837 units
- Distribution
- NC, ID, Belgium, Switzerland, Spain, Germany, Australia, France, Italy
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip arthroplasty in primary or revision surgery.. Recalled by Medacta Usa Inc. Units affected: 837 units.
Why was this product recalled? ▼
Complaint monitoring noted a trend of packaging being breached for the MiniMAX Stem.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 31, 2018. Severity: Moderate. Recall number: Z-0196-2019.
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