FDA Adverse Event Injury Summary report: N

COCR CABLE SLEEVE

MDR report key: 8062499 · Received November 12, 2018

Report

Report Number
0001825034-2018-10555
Event Type
Injury
Date Received
November 12, 2018
Report Date
November 12, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HRS
PMA / PMN Number
K982545
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: 11-301312 ARCOS CON 491000; 11-300922 ARCOS DISTAL TAPER 501080; PT-106056 RENG RINGLOC SHELL 150750; 11-107323 FREEDOM STANDARD LINER 363880; 11-107018 FREEDOM CONSTRAINED HEAD 968260; 120002 COCR TROCH CABLE 516680; 120005 COCR CABLE SLEEVE 609390 (QTY 4); 103531 PROFILE SCREW 930580 (QTY 5). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILE ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-10545; 0001825034-2018-10547;0001825034-2018-10548;0001825034-2018-10549;0001825034-2018-10550; 0001825034-2018-10553.

Description of Event or Problem · 1

IT WAS REPORTED PATIENT EXPERIENCED RIGHT HIP DRAINAGE WITH DIVERTICULITIS AND UTI AT AN UNKNOWN AMOUNT OF TIME POST RIGHT HIP REVISION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
898964 COCR CABLE SLEEVE PROSTHESIS, TRAUMA HRS ZIMMER BIOMET, INC. N/A 609390

Patients

Seq Age Sex Outcome Treatment
1 Other