9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TSRH SPINAL FIXATION SYSTEM
FDA Adverse Event
Injury
·SOFAMOR DANEK MANUFACTURING·Product code KWQ·January 5, 2000
C.R. BARD
FDA Adverse Event
Injury
·BARD UROLOGICAL DIVISION·Product code KOD·February 9, 1995
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC., SAN ANGELO·Product code GAM·May 5, 2000
INTRA-AORTIC BALLOON PUMP
FDA Adverse Event
Malfunction
·ST. JUDE CARDIAC ASSIST DIVISION·Product code DSP·March 7, 1995
RESERVOIR 1.8ML MMT-326A
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 10, 2014
HEARTSTART FRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 3, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·July 14, 2011
11.0MM CANNULATED CUTTER
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWJ·November 27, 2017
ALPHA I INFLATABLE PENILE PROSTHESIS
FDA Adverse Event
Injury
·MENTOR UROLOGY, INC.·Product code FHW·October 17, 1997