FDA Adverse Event Injury Summary report: N

TAPERLOC POR RED/DIST 13.5X147

MDR report key: 8101075 · Received November 26, 2018

Report

Report Number
0001825034-2018-10867
Event Type
Injury
Date Received
November 26, 2018
Date of Event
January 10, 2013
Report Date
April 9, 2019
Manufacturer
ZIMMER BIOMET, INC.
Product Code
LPH
PMA / PMN Number
K921301
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NV, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

REPORTED EVENT WAS CONFIRMED BY REVIEW OF MEDICAL RECORDS. POSTOPERATIVE VISIT NOTES STATE THAT THE PATIENT WAS FOUND TO HAVE CELLULITIS ABOUT THE L HIP WOUND, AND WAS TREATED WITH ANTIBIOTICS. THE CELLULITIS CONTINUED FOR APPROXIMATELY 2 WEEKS AFTER TREATMENT. THE DEVICE HISTORY RECORDS WERE REVIEWED AND NO RELATED DEVIATIONS/ ANOMALIES WERE IDENTIFIED THAT AFFECT THE REPORTED EVENT. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED WITH THE INFORMATION PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Description of Event or Problem · 0

NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

Additional Manufacturer Narrative · 1

(B)(4). MEDICAL DEVICES: 54ODX48ID MAGNUM ABX PF CUP #US157854 LOT 072830, 32MM MOD HEAD COCR -6MM NECK # 163667 LOT 196450. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-10865 AND 0001825034-2018-10866. IT IS UNKNOWN IF PRODUCT WILL BE RETURNING TO ZIMMER BIOMET AND THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT CELLULITIS WAS NOTED ABOUT THE LEFT HIP WOUND APPROXIMATELY 2 MONTHS POST REVISION AND TREATED WITH ANTIBIOTICS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
942402 TAPERLOC POR RED/DIST 13.5X147 PROSTHESIS HIP LPH ZIMMER BIOMET, INC. N/A 534610

Patients

Seq Age Sex Outcome Treatment
1 39 YR Other