FDA Adverse Event Injury Summary report: N

UNK TISSUE EXPANDER

MDR report key: 14605173 · Received June 6, 2022

Report

Report Number
9617229-2022-10278
Event Type
Injury
Date Received
June 6, 2022
Report Date
June 6, 2022
Manufacturer
ALLERGAN (COSTA RICA)
Product Code
LCJ
PMA / PMN Number
K862203
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

ARTICLE CITATION: SATOKO ONISHI, YOSHIKAZU INOUE, MAKI INUKAI, TAKAYUKI OKUMOTO, PREVENTING INFECTION AFTER SYNTHETIC EXPANDER IMPLANTATION IN PATIENTS UNDERGOING BREAST RECONSTRUCTION, FUJITA MEDICAL JOURNAL, 2022, VOLUME 8, ISSUE 2, PAGES 42-45, RELEASED ON J-STAGE MAY 01, 2022, ADVANCE ONLINE PUBLICATION AUGUST 20, 2021, ONLINE ISSN 2189-7255, PRINT ISSN 2189-7247, HTTPS://DOI.ORG/10.20407/FMJ.2020-029, HTTPS://WWW.JSTAGE.JST.GO.JP/ARTICLE/FMJ/8/2/8_2020-029/_ARTICLE/-CHAR/EN. THE EVENTS OF INFECTION AND NECROSIS 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: INFECTION AND NECROSIS.

Description of Event or Problem · 0

THROUGH JOURNAL ARTICLE "PREVENTING INFECTION AFTER SYNTHETIC EXPANDER IMPLANTATION IN PATIENTS UNDERGOING BREAST RECONSTRUCTION" ONE PATIENT REPORTED "INFECTION, SKIN AROUND THE POSTOPERATIVE WOUND HAD BECOME NECROTIC, RESULTING IN AN ULCER" AS WELL AS "INFLAMMATORY SIGNS DUE TO CHEST ERYTHEMA AS WELL AS FEVER" AND "(B)(6)." THIS IS FOR AN UNKNOWN SIDE. DEVICE HAS BEEN EXPLANTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
158733 UNK TISSUE EXPANDER EXPANDER, SKIN, INFLATABLE LCJ ALLERGAN (COSTA RICA) NI

Patients

Seq Age Sex Outcome Treatment
1 Female Required Intervention