FDA Adverse Event Injury Summary report: N

M2A-MAGNUM TPR INSRT

MDR report key: 9321283 · Received November 14, 2019

Report

Report Number
0001825034-2019-05137
Event Type
Injury
Date Received
November 14, 2019
Date of Event
September 4, 2008
Report Date
January 29, 2020
Manufacturer
ZIMMER BIOMET, INC.
Product Code
KWA
UDI-DI
00880304428010
PMA / PMN Number
K042037
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL 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 ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: US157850-M2A-MAGNUM PF CUP-167780, 157444-M2A-MAGNUM MOD HD-134600, X12-171313-INTEGRAL/X POR-299620. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 -2019 -05135, 0001825034 -2019 -05136.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT UNDERWENT AN INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT UNDERWENT A REVISION DUE TO UNKNOWN REASONS A YEAR LATER. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1115449 M2A-MAGNUM TPR INSRT PROSTHESIS, HIP KWA ZIMMER BIOMET, INC. NI 228310 00880304428010

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R