FDA Adverse Event Injury Summary report: N

VANG XP INLK PRI TIB TRAY 65MM

MDR report key: 7292322 · Received February 23, 2018

Report

Report Number
0001825034-2018-01384
Event Type
Injury
Date Received
February 23, 2018
Report Date
February 23, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
PMA / PMN Number
PK132873
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4) MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT. PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-01383, 0001825034-2018-01385, 0001825034-2018-01386. CONCOMITANT MEDICAL PRODUCTS: 195907 VANG XP INLK FEMORAL RT 57.5 LOT 516580, 195773 VGXP XP LAT TIB BRG RT 10X63 LOT 811160, 195606 VGXP AS TIB BRG RM/LL 10X67 LOT 825180. (B)(6). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION IS REQUIRED AS NO WERE TRENDS IDENTIFIED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT 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. DEVICE REMAINS IMPLANTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT HAD A KNEE IMPLANT AND HAD MENTIONED SOME PROBLEMS WALKING, WASHING/DRESSING, MODERATE PAIN, PAIN DURING STANDING UP, OCCASIONAL LIMPING, IMPOSSIBILITY TO KNEEL, EXTREME DIFFICULTY WALKING DOWN STAIRS, TROUBLED SLEEP DUE TO PAIN, AND INTERFERENCE WITH USUAL ACTIVITIES DURING HER 6 MONTH FOLLOW UP VISIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
137195 VANG XP INLK PRI TIB TRAY 65MM PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 963440

Patients

Seq Age Sex Outcome Treatment
1 80 YR Other