FDA Adverse Event Injury Summary report: N

MAESTRO TOTAL WRIST CARPAL PLATE 9X37 AUG 6

MDR report key: 7758288 · Received August 7, 2018

Report

Report Number
0001825034-2018-04644
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 MEDICAL PRODUCTS: 180181 MAESTRO RADIAL STEM 6.0 X 40 MM 635990, 180120 MAESTRO CAPITATE STEM 6 X 12 MM 303280, 180151 MAESTRO RAD W/BRG 7X15 7.5 RT 294070, 180063 MAESTRO CARPAL HEAD 7 X 15 MM STD 961010, 113846 TITANIUM SCREW LOW PROF 5 X 30 MM 472030, 113843 TITANIUM SCREW LOW PROF 5 X 15 MM 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, 0001825034-2018-04648.

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
597521 MAESTRO TOTAL WRIST CARPAL PLATE 9X37 AUG 6 PROSTHESIS, WRIST JWJ ZIMMER BIOMET, INC. N/A 697940

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R