FDA Adverse Event Injury Summary report: N

UNK GLENOID HEAD

MDR report key: 10134392 · Received June 9, 2020

Report

Report Number
0001822565-2020-02060
Event Type
Injury
Date Received
June 9, 2020
Date of Event
January 8, 2020
Report Date
June 8, 2020
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HSD
PMA / PMN Number
NI
Removal / Correction Number
NI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001822565-2020-00414. 0001822565-2020-00415. 0001822565-2020-02059. 0001822565-2020-02061. 0001822565-2020-02062. CONCOMITANT MEDICAL PRODUCTS: UNK POLY, ITEM# 00434901413, LOT#64141262. UNK BASEPLATE, UNK SCREW, UNK SCREW. NO PRODUCT WAS RETURNED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. INSUFFICIENT INFORMATION PROVIDED. UNABLE TO PERFORM A COMPATIBILITY CHECK. MEDICAL RECORDS WERE NOT PROVIDED. PART AND LOT IDENTIFICATION ARE NECESSARY FOR REVIEW OF DEVICE HISTORY RECORDS FOR OTHER DEVICES, NEITHER WERE PROVIDED. A DEFINITIVE ROOT CAUSE COULD NOT BE DETERMINED. 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

IT WAS REPORTED THE PATIENT WAS IMPLANTED WITH A REVERSE SHOULDER OVER A YEAR AGO. SUBSEQUENTLY, THE PATIENT WAS REVISED A COUPLE OF MONTHS AGO DUE TO THE POLY DISENGAGING FROM THE STEM. A SECOND REVISION WAS RECENTLY PERFORMED DUE TO ANOTHER DISENGAGED POLY AND POSSIBLE INFECTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
595556 UNK GLENOID HEAD PROSTHESIS, EXTREMITIES HSD ZIMMER BIOMET, INC. NI NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R