FDA Adverse Event Injury Summary report: N

VERSA-DIAL/COMP TI STD TAPER

MDR report key: 8382179 · Received March 1, 2019

Report

Report Number
0001825034-2019-00926
Event Type
Injury
Date Received
March 1, 2019
Date of Event
September 11, 2018
Report Date
June 24, 2019
Manufacturer
ZIMMER BIOMET, INC.
Product Code
MBF
PMA / PMN Number
K060716
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

(B)(4). THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL AND/OR CORRECTED INFORMATION. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. 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.

Description of Event or Problem · 0

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

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: PART # 113627, LOT # 292310, COMP PRIMARY STEM 7MM MINI; PART # 115310, LOT # 990660, COMP RVRS SHLDR GLNSP STD 36MM; PART # 110005273, LOT # 184150, COMP CNV GLEN BASE NON HA; PART # XL-115363, LOT # 588250 OR 145510, ARCOM XL 44-36 STD HMRL BRNG; PART # 115375, O5 115370, LOT # 822460, OR 272100 COMP RVS TRAY CO 44MM; PART # 115395, LOT # 650420 COMP RVS CNTRL 6.5X25MM ST/RST; PART # 180551, LOT # 969080, COMP LK SCR 3.5HEX 4.75X20 ST; PART # 180552, LOT # 715590, COMP LK SCR 3.5HEX 4.75X25 ST; PART # 405883, LOT # 538650, COMP RVS 3.2MM DRL; PART # 405800, LOT # 905620, COMP. REV SHLDR 9 IN STEINMANN; PART # 405889, LOT # 538820, COMP RVS 2.7MM DIA DRL; PART # 110005237, LOT # 509950, COMP CONV GLEN LINER E1. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2019 -00920, 0001825034 -2019 -00921, 0001825034 -2019 -00922, 0001825034 -2019 -00923, 0001825034 -2019 -00924, 0001825034 -2019 -00925. NOT RETURNED TO MANUFACTURER.

Description of Event or Problem · 1

IT HAS BEEN REPORTED THAT PATIENT IS SUFFERING FROM CHRONIC PAIN AND NON FUNCTIONING JOINT (9) NINE MONTHS POST REVISION SURGERY. PATIENT IS UNDERGOING SEEKING CARE UNDER A PAIN MANAGEMENT SPECIALIST. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
174456 VERSA-DIAL/COMP TI STD TAPER PROSTHESIS, SHOULDER MBF ZIMMER BIOMET, INC. N/A 120880

Patients

Seq Age Sex Outcome Treatment
1 56 YR Required Intervention| S