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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA AMISTEM H HA COATED LAT STEM SIZE 2; CEMENTLESS HIP STEM
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MEDACTA INTERNATIONAL SA AMISTEM H HA COATED LAT STEM SIZE 2; CEMENTLESS HIP STEM Back to Search Results
Catalog Number 01.18.142
Health Effect - Clinical Code Joint Disorder (2373)
Date of Event 12/13/2017
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
Batch review performed on 05 january 2018: lot 153982: (b)(4) items manufactured and released on 09 december 2015.Expiration date: 2020-11-24.No anomalies found related to the issue.To date, (b)(4) items of the same lot have been already sold without any similar reported event.
 
Event or Problem Description
The patient complained hip laxity.1 year and 8 months after primary the surgeon detected a stem subsidence and revised successfully the patient swapping the stem, the head and the liner.
 
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Brand Name
AMISTEM H HA COATED LAT STEM SIZE 2
Common Device Name
CEMENTLESS HIP STEM
Manufacturer (Section D)
MEDACTA INTERNATIONAL SA
strada regina
castel san pietro, 6874
SZ  6874
MDR Report Key7185279
Report Number3005180920-2017-00827
Device Sequence Number1496832
Product Code LZO
UDI-Device Identifier07630030804182
UDI-Public07630030804182
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K093944
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2016
Device Explanted Year2017
Reporter Type Manufacturer
Report Source other
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 01/12/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Expiration Date11/24/2020
Device Catalogue Number01.18.142
Device Lot Number153982
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 12/13/2017
Initial Report FDA Received Date01/12/2018
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age54 YR
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