FDA Adverse Event Injury Summary report: N

UNK MAMMARY IMPLANT

MDR report key: 11125774 · Received January 6, 2021

Report

Report Number
9617229-2020-22863
Event Type
Injury
Date Received
January 6, 2021
Date of Event
August 21, 2019
Report Date
January 6, 2021
Manufacturer
ALLERGAN (COSTA RICA)
Product Code
FWM
PMA / PMN Number
P990074
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ARTICLE CITATION: FAT GRAFTING AFTER IMPLANT REMOVAL DUE TO ANAPLASTIC LARGE CELL LYMPHOMA MAY MIMIC RECURRENCE. NIR BITTERMAN MD, PAULA SIMOVIZ MD, TAMAR TADMOR MD, LIHI TZUR MD, NOAM CALDERON MD, AND OHAD BEN-NUN MD. IMAJ ¿VOL21¿ AUGUST2019. THE EVENTS OF ¿SEROMA-LATE", "CAPSULAR CONTRACTURE¿, AND "LYMPHOMA" ARE PHYSIOLOGICAL COMPLICATIONS AND ANALYSIS OF THE DEVICE GENERALLY DOES NOT ASSIST ALLERGAN IN DETERMINING A PROBABLE CAUSE FOR THESE EVENTS. FURTHER INFORMATION FROM THE REPORTER REGARDING EVENT, PRODUCT, OR PATIENT DETAILS HAS BEEN REQUESTED. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. REASON FOR REOPERATION: SEROMA-LATE, CAPSULAR CONTRACTURE, BAKER GRADE UNKNOWN, AND BIA-ALCL DATE OF ALCL DIAGNOSIS: 10 YEARS FROM DEVICE IMPLANT.

Description of Event or Problem · 1

JOURNAL ARTICLE: "FAT GRAFTING AFTER IMPLANT REMOVAL DUE TO ANAPLASTIC LARGE CELL LYMPHOMA MAY MIMIC RECURRENCE.". THE ARTICLE REPORTS A PATIENT DIAGNOSED WITH BIA-ALCL. THE PATIENT PRESENTED WITH ¿SEROMA AND CAPSULAR CONTRACTURE¿ AND WAS TREATED WITH ¿CAPSULECTOMY, DEVICE REMOVAL AND CHEMOTHERAPY¿. PATHOLOGICAL MARKERS CONFIRMING ALCL HAVE NOT BEEN RECEIVED. SIDE UNKNOWN. DEVICE HAS BEEN EXPLANTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
19770 UNK MAMMARY IMPLANT PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE FWM ALLERGAN (COSTA RICA) NI

Patients

Seq Age Sex Outcome Treatment
1 63 YR Required Intervention