133 results
·
67ms
·
Sources: EU EUDAMED, US FDA
DIAGNOSTIC PRODUCTS CORP. RIA CONTROL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
IMMULITE REAGENT WEDGE
FDA Adverse Event
Injury
·DIAGNOSTIC PRODUCTS CORP·Product code JJQ·November 21, 2002
IMMULITE 2000 ANALYZER
FDA Adverse Event
DPC INSTRUMENT SYSTEMS DIVISIONS·Product code JJQ·August 11, 2003
IMMULITE 2000 ANALYZER
FDA Adverse Event
DPC INSTRUMENT SYSTEMS DIVISIONS·Product code JJQ·January 15, 2003
DIAGNOSTIC PRODUCT CORP
FDA Adverse Event
Malfunction
·*·Product code JJQ·January 23, 2006
IMMULITE 2000 INTACT PTH
FDA Adverse Event
Malfunction
·DIAGNOSTIC PRODUCTS CORP.·Product code JJQ·March 17, 2004
THIRD GENERATION TSH ASSAY
FDA Adverse Event
Malfunction
·DIAGNOSTIC PRODUCTS CORP·Product code JLW·May 16, 2006
DPC IMMULITE
FDA Adverse Event
Malfunction
·DIAGNOSTIC PRODUCTS CORP.·Product code JJE·May 3, 2004
IMMULITE 2000 H. PYLORI IGG
FDA Adverse Event
Malfunction
·DIAGNOSTIC PRODUCTS CORP.·Product code LYR·April 18, 2001
DPC IMMULITE H PYLORI IGG
FDA Adverse Event
Other
·DIAGNOSTIC PRODUCTS CORP·Product code KTO·May 8, 2001
IMMULITE 2000 Total Testosterone Kit
FDA Recall
Terminated
·Diagnostic Products Corp.·Product code CDZ·January 3, 2006
Immulite/ Immulite 1000 Carcinoembryonic Antigen (CEA) LKCE1 lot 302 and 303
FDA Recall
Terminated
·Diagnostic Products Corp·Product code DHX·May 26, 2005
Immulite 2500 insulin Kit
FDA Recall
Terminated
·Diagnostic Products Corp·Product code CFP·November 19, 2004
Immulite 2000 H. pylori IgG Kit lot 118 (L2KHQ6, 600 test size kit)
FDA Recall
Terminated
·Diagnostic Products Corp·Product code LYR·July 31, 2003
IMMULITE 2000 Intact PTH kit
FDA Recall
Terminated
·Diagnostic Products Corp·Product code CEW·February 23, 2004
Immulite 1000 CEA Catalog No. LKCE1
FDA Recall
Terminated
·Diagnostic Products Corp·Product code DHX·May 3, 2004
IMMULITE 2000 Vitamin B12 Kit, Catalog # L2KVB2, L2KVB6, kit lot 186.
FDA Recall
Terminated
·Diagnostic Products Corp·Product code CDD·January 24, 2005
DPC IMMULITE 1000
FDA Adverse Event
Malfunction
·DIAGNOSTICS PRODUCTS CORP·Product code KHO·September 13, 2004
QUATTRO PREMIER XE MASS SPECTROMETER
FDA Adverse Event
Death
·WATERS CORP·Product code OQS·March 24, 2010
LIFESYNC LEADWEAR
FDA Adverse Event
Other
·LIFESYNC CORPORATION·Product code DSA·January 9, 2009