22 results · 56ms · Sources: EU EUDAMED, US FDA

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GEL-FILLED MAMMARY PROSTHESIS

FDA Adverse Event
Injury ·AMERICAN HEYER-SCHULTE·Product code FTR·March 6, 1998

HEYER-SCHULTE CORP.

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP.·Product code FWM·April 23, 1997

KERRISON RONGEUR

FDA Adverse Event
Other ·REDMOND NEUROTECHNOLOGIES CORP.·Product code HAE·June 9, 1997

HEYER-SCHULTE

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP.·Product code FTR·July 22, 2004

PROSTHESIS, MAMMARY, INTERNAL

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP.·Product code FTR·July 13, 1994

HEYER SCHULTE

FDA Adverse Event
Injury ·HEYER SCHULTE CORP.·Product code FTR·May 13, 1998

MAMMARY PROSTHESIS

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP·Product code FTR·December 21, 1999

HEYER-SCHULTE CORPORATION

FDA Adverse Event
Malfunction ·HEYER-SCHULTE CORP.·Product code FWM·November 25, 1998

HEYER-SCHULTE

FDA Adverse Event
Malfunction ·HEYER-SCHULTE CORP.·Product code FTR·March 22, 1999

AMERICAN HEYER-SCHULTE

FDA Adverse Event
Injury ·AMERICAN HEYER-SCHULTE CORP.·Product code FTR·August 7, 1996

HYER SCHULTE BREAST IMPLANTS

FDA Adverse Event
Injury ·HEYER SCHULTE CORP, SUBSIDARY·Product code FTR·July 21, 1994

UNKNOWN

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP. (HEYER-SCHULTE)·Product code FTR·February 4, 1994

HEYER SCHULTE

FDA Adverse Event
Injury ·HEYER SCHULTE/BAXTER HEALTHCARE CORP.·Product code FTR·March 20, 1998

SILICONE GEL BREAST IMPLANT

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP. HEYER SCHULTE·Product code FTR·April 21, 1998

NO RECORDS

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP. HEYER SCHULTE·Product code FTR·April 21, 1998

SILICONE GEL BREAST IMPLANT

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP. HEYER SCHULTE·Product code FTR·April 24, 1998

SILICONE GEL BREAST IMPLANTS

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP. HEYER SCHULTE·Product code FTR·April 21, 1998

HEYER-SCHULTE

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP. DIV. OF AMERICAN HOSP. SUPPLY·Product code FTR·January 9, 1998

HEYER-SCHULTE

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP. SUB OF AMERICAN HOSPITAL SUPPLY CORP.·Product code FWM·December 26, 1996

HEYER-SCHULTE

FDA Adverse Event
Injury ·HEYER-SCHULTE CORP SUB OF AMERICAN HOSP SUPPLY CORP·Product code FWM·August 8, 2001