7 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ULTRA DRIVE 6MM PLUG PULLER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDX·July 20, 2022
PORTEX BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INT'L LTD.·Product code JOH·March 5, 2013
ACCU-CHEK FLEXLINK PLUS
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FRN·March 22, 2011
INVACARE POWER WHEELCHAIR
FDA Adverse Event
Injury
·INVACARE CORPORATION - MANUFACTURING FACILITY·Product code ITI·April 18, 2008
OXFORD PARTIAL KNEE SYSTEM ANATOMIC MENISCAL BEARING ARCOM RIGHT MEDIAL
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·June 23, 2017
2710 CLEARTRACE LT
FDA Adverse Event
Other
·CONMED CORPORATION·Product code GXY·April 13, 2007
KINETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·April 16, 2012