FDA Adverse Event Injury Summary report: N

VGXP XP INLK PRI TIB TRAY 75MM

MDR report key: 7291829 · Received February 23, 2018

Report

Report Number
0001825034-2018-01341
Event Type
Injury
Date Received
February 23, 2018
Date of Event
June 7, 2016
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
MN, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT PRODUCTS: PART 195911, LOT 244250- GXP INTLK FEMORAL RT 67.5. PART 195780, LOT 057810- VGXP XP E1 TIB BRG RL 10X71. PART 195850, LOT UNK- VGXP XP E1 TIB BRG RM 10X71. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: MFR 0001825034-2018-01340, MFR 0001825034-2018-01342, MFR 0001825034-2018-01343. 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 TRENDS WERE IDENTIFIED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORT EVENT WAS NOT REPORTED. THERE ARE WARNINGS IN THE PACKAGE INSERT THAT THIS TYPE OF EVENT CAN OCCUR AND RISKS ARE ADDRESSED IN RISK DOCUMENTATION. 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 · 1

CLINICAL STUDY (B)(6) - PATIENT EXPERIENCED POST-OPERATIVE PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
134950 VGXP XP INLK PRI TIB TRAY 75MM PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 592640

Patients

Seq Age Sex Outcome Treatment
1 71 YR Other