658 results · 24ms · Sources: EU EUDAMED, US FDA

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BREAST IMPLANTS

FDA Adverse Event
Injury ·ALLERGAN·Product code FTR·November 1, 2019

SHERLOCK 3CG SENSOR (RADEL)

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·June 24, 2021

ALLERGAN NATRELLE BIO TEXTURED IMPLANTS

FDA Adverse Event
Injury ·ALLERGAN·Product code FTR·December 13, 2019

BREAST IMPLANT

FDA Adverse Event
Injury ·MENTOR·Product code FWM·November 23, 2015

ALLODERM

FDA Adverse Event
Injury ·ALLERGAN / LIFECELL·Product code FTL·April 3, 2019

NATRELLE 410

FDA Adverse Event
Injury ·ALLERGAN·Product code FTR·October 12, 2017

ALLERGAN NATTELLE 410 HIGHLY COHESIVE TEXTURED GEL IMPLANTS

FDA Adverse Event
Injury ·ALLERGAN·Product code FTR·April 9, 2019

MENTOR MEMORY GEL BREAST IMPLANT

FDA Adverse Event
Injury ·JOHNSON AND JOHNSON / MENTOR WORLDWIDE LLC·Product code FTR·June 13, 2019

MEMORY SHAPE GEL TEXTURED

FDA Adverse Event
Injury ·MENTOR·Product code FTR·May 19, 2017

SALINE IMPLANTS

FDA Adverse Event
Injury ·UNK·Product code FWM·January 30, 2019

COAPT SYSTEMS, INC

FDA Adverse Event
Injury ·*·Product code MAI·November 30, 2007

SMOOTH RND HIGH GEL MAMMARY PROSTH

FDA Adverse Event
Injury ·MENTOR·Product code FTR·March 27, 2019

STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FTR·December 13, 2019

INAMED

FDA Adverse Event
Injury ·Product code FWM·March 6, 2008

TEXTURED 390CC BREAST IMPLANTS (3RD SET) MADE IN 1990'S

FDA Adverse Event
Injury ·ALLERGAN / MCGHAN·Product code FWM·September 10, 2019

STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FTR·December 17, 2019

PAK12

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MYP·September 15, 2015

PAKAUTO

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MYP·October 24, 2018

GTI TEST KITS

FDA Adverse Event
Malfunction ·GTI DIAGNOSTICS·Product code MYP·December 23, 2010

PAKPLUS

FDA Adverse Event
Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MYP·February 8, 2018