10,000 results
·
97ms
·
Sources: EU EUDAMED, US FDA
BD Medical – Pharmaceutical Systems,Becton, Dickinson and Company
Manufacturer
🇺🇸 United States·2 Importers
BD MEDICAL SYSTEMS
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FOZ·January 2, 2004
BD MEDICAL SYSTEMS, INC.
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS, INC.·Product code FOZ·October 13, 2004
BD Beaver Slit Blade 3.0mm Straight Part Number: 375521 The BD Beaver Slit Blade is used to perform the main incision through which instruments are inserted during cataract surgery.
FDA Recall
Terminated
·Bd Medical Systems·June 24, 2010
Becton Dickinson France SAS
Authorized representative
🇫🇷 France·2 Manufacturers
BD FIRST PICC
FDA Adverse Event
BD MEDICAL SYSTEMS·Product code LJS·February 5, 2010
BD INTEGRA SYRINGE W/DETACHABLE NEEDLE
FDA Adverse Event
Injury
·BD MEDICAL SYSTEMS·Product code MEG·August 12, 2015
INSYTE AUTOGUARD
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FOZ·February 4, 2004
BD POSIFLUSH
FDA Adverse Event
Injury
·BD MEDICAL SYSTEM·Product code NGT·January 29, 2004
BD INSYTE AUTOGUARD
FDA Adverse Event
Injury
·BD MEDICAL SYSTEMS·Product code FOZ·March 25, 2004
FIRST CATH 1.9 FRENCH
FDA Adverse Event
Injury
·BD MEDICAL SYSTEMS·Product code DQO·February 22, 2002
BD INSYTE AUTOGUARD
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FOZ·March 4, 2002
BD ANGIOCATH
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FOZ·January 7, 2002
BD INSYTE AUTOGUARD
FDA Adverse Event
BD MEDICAL SYSTEMS·Product code FOZ·September 30, 2003
BD INSYTE AUTOGUARD 18 GA 1.16 IN
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FMI·September 12, 2003
BD INSTYE AUTOGUARD
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FOZ·September 10, 2003
BD INSYTE AUTOGUARD 18 GA 1.16 IN
FDA Adverse Event
BD MEDICAL SYSTEMS·Product code FOZ·September 12, 2003
BD INSYTE AUTOGUARD H3120A
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FMI·September 15, 2003
INTRODUCER NEEDLE, U-WING
FDA Adverse Event
Malfunction
·BD MEDICAL SYSTEMS·Product code FOZ·July 6, 2000
L-CATH CATHETER SYSTEM
FDA Adverse Event
Injury
·BD MEDICAL SYSTEMS·Product code DQO·July 6, 2000