FDA Adverse Event Injury Summary report: N

TRILOGY ACETABULAR POLYETHYLENE LINER

MDR report key: 2033469 · Received March 24, 2011

Report

Report Number
1822565-2011-00737
Event Type
Injury
Date Received
March 24, 2011
Report Date
August 27, 2009
Manufacturer
ZIMMER, INC.
Product Code
LPH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO DEVICES OR PHOTOS WERE RECEIVED; THEREFORE, THE CONDITION OF THE COMPONENTS IS UNK. SURGICAL NOTES WERE NOT PROVIDED. X-RAYS WERE NOT PROVIDED; IT IS UNK WHETHER THE COMPONENTS WERE IMPLANTED WITH THE CORRECT FIT AND ORIENTATION AS PER THE SURGICAL TECHNIQUE. PT FACTORS THAT MAY AFFECT THE PERFORMANCE OF THE COMPONENTS SUCH AS BONE QUALITY, HEIGHT/WEIGHT, ACTIVITY LEVEL, TYPE OF ACTIVITY (LOW IMPACT VS. HIGH IMPACT) ARE UNK. THERE IS INSUFFICIENT INFO TO PERFORM A PROBABLE CAUSE ANALYSIS. REVIEW OF THE DEVICE HISTORY RECORDS DID NOT FIND ANY DEVIATIONS OR ANOMALIES. IT IS NOT SUSPECTED THAT THE PRODUCT FAILED TO MEET SPECIFICATIONS. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY EVIDENCE OF PRODUCT CONTRIBUTION TO THE REPORTED PROBLEM. BASED ON THE INVESTIGATION, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. SHOULD ADDITIONAL SUBSTANTIVE INFO BE RECEIVED, THE COMPLAINT WILL BE REOPENED. THIS MDR WAS IDENTIFIED DURING AN INTERNAL REVIEW TO MEET REPORTING REQUIREMENTS AND THEREFORE, IS BEING FILED LATE.

Description of Event or Problem · 1

IT IS REPORTED THAT THE PT HAS PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRILOGY ACETABULAR POLYETHYLENE LINER LPH ZIMMER, INC. 60533852

Patients

Seq Age Sex Outcome Treatment
1 Other LOT #60518673| MANUFACTURED AT ZIMMER (B)(4)| LOT #60568730, MANUFACTURED AT ZIMMER (B)(4)| (B)(4)| BONE SCREW, CATALOG #00625006530, LOT #60517073| TABECULAR METAL FEMORAL, CATALOG #00796401200| TRILOGY ACETABULAR SHELL, CATALOG #00620005022| LOT #UNKNOWN| VERSYS HIP FEMORAL HEAD, CATALOG #00801803202