FDA Adverse Event Injury Summary report: N

MAESTRO TOTAL WRIST CARPAL HEAD 7X15MM STD

MDR report key: 7758305 · Received August 7, 2018

Report

Report Number
0001825034-2018-04648
Event Type
Injury
Date Received
August 7, 2018
Date of Event
May 20, 2011
Report Date
August 7, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWJ
PMA / PMN Number
PK042032
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT PRODUCTS: 180181 MAESTRO RADIAL STEM 6.0X40MM 635990; 180120 MAESTRO CAPITATE STEM 6X12MM 303280; 180151 MAESTRO RAD W/BRG 7X15 7.5 RT 294070; 180103 MAESTRO CARP PLATE 9X37 AUG 6 697940; 113846 TITANIUM SCREW LOW PROF 5X30MM 472030; 113843 TITANIUM SCREW LOW PROF 5X15MM 349570. THE COMPLAINT CANNOT BE CONFIRMED WITH LIMITED INFORMATION RECEIVED. REVIEW OF DEVICE HISTORY RECORDS FOUND THESE UNITS WERE RELEASED TO DISTRIBUTION WITH NO DEVIATIONS OR ANOMALIES. ROOT CAUSE COULD NOT BE DETERMINED WITH THE INFORMATION PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2018 - 04638 , 0001825034 - 2018 - 04639 , 0001825034 - 2018 - 04641 , 0001825034 - 2018 - 04644.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A WRIST REVISION DUE TO UNKNOWN REASONS FIVE YEARS POST PRIMARY SURGERY. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
596771 MAESTRO TOTAL WRIST CARPAL HEAD 7X15MM STD PROSTHESIS, WRIST JWJ ZIMMER BIOMET, INC. N/A 961010

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R