4,004 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LFX-SI
FDA UDI
AGILENT TECHNOLOGIES, INC.·05700574035099·Automated Microscope
STENOSCOPE
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·December 18, 2009
LFX GENERATOR
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code IZO·July 27, 1998
LFX GENERATOR
FDA Adverse Event
Injury
·GE MEDICAL SYSTEMS·Product code IZO·October 17, 1997
LFX GENERATOR
FDA Adverse Event
Death
·GENERAL ELECTRIC CO.·Product code IZO·April 27, 1998
TriActiv FX Embolic Protection System 7F, Catalog numbers 60040-02 (has 190 cm guidewire) and 60040-03 (has 300 cm guidewire). The devices are comprised of four principal components including the ShieldWire Balloon Guidewire, the Shieldwire Inflator, the FX or LFX Catheter, and the AutoStream Flow Control.
FDA Recall
Terminated
·Kensey Nash Corp·Product code FRO·March 28, 2007
Sterile Procedural Trays, labeled as the following: a. KNEE ARTHROSCOPY CDS-LF b. ARTHROSCOPY CDS c. ARTHROSCOPY LV - EDOC PACK-LF d. ARTHROSCOPY PACK-LF e. ARTHROSCOPY PACK f. ARTHRO PACK-LF g. ARTHROSCOPY PACK-LF h. ARTHROSCOPY PACK-LF i. ARTHROSCOPY KNEE TRAY-LF j. ARTHROSCOPY PACK-LF k. ARTHROSCOPY BASIN PACK-LF l. ARTHROTOMY PACK-LF m. ARTHROSCOPY PACK-LF n. ARTHROSCOPY PACK o. ARTHROSCOPY PACK p. ARTHROSCOPY PACK q. ARTHROSCOPY PACK - LF r. SC ARTHROSCOPY PACK s. ARTHROSCOPY PACK-LF t. ARTHROSCOPY PACK u. ARTHROSCOPY PACK v. ARTHROSCOPY PACK w. OSC ARTHROSCOPY PK-LF x. ARTHROSCOPY PACK y. ARTHROSCOPY PACK z. ARTHROSCOPY PACK aa. ARTHROSCOPY PACK bb. ARTHROSCOPY PACK cc. KNEE ARTHROSCOPY PACK dd. KNEE ARTHROSCOPY PACK ee. SHOULDER ARTHROSCOPY PACK ff. SHOULDER ARTHROSCOPY gg. ARTHROSCOPY PACK hh. ARTHROSCOPY PACK ii. ARTHROSCOPY PACK jj. ARTHROSCOPY PACK kk. ARTHROSCOPY PACK ll. ARTHROSCOPY PACK-LF mm. ARTHROSCOPY KNEE nn. ARTHROSCOPY PACK oo. HIP ARTHROSCOPY PACK pp. ARTHROSCOPY PACK qq. MG NS KNEE ARTHROSCOPY PACK rr. KNEE ARTHROSCOPY PACK ss. ARTHROSCOPY PACK tt. ARTHROSCOPY-LF uu. ARTHROSCOPY KIT vv. SHOULDER ARTHROSCOPY ww. KNEE ARTHROSCOPY xx. ARTHROSCOPY PACK
FDA Recall
Open, Classified
·MEDLINE INDUSTRIES, LP Northfield·Product code OII·November 17, 2022
VIDAS® RUB IGG II ASSAY
FDA Adverse Event
Malfunction
·BIOMERIEUX SA·Product code LFX·September 29, 2015
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code LFX·March 21, 2012
UNICEL¿ DXL800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code LFX·March 8, 2012
AXSYM RUBELLA IGM
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LFX·March 11, 2009
ADVIA CENTAUR RUBELLA G (RUB G) ASSAY
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LFX·February 17, 2009
ADVIA CENTAUR XP RUBELLA M (RUB M) ASSAY
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LFX·May 23, 2014
IGG ANTIBODIES TO RUBELLA VIRUS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFX·June 24, 2014
IGG ANTIBODIES TO RUBELLA VIRUS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFX·June 24, 2014
ADVIA CENTAUR XP RUBELLA G (RUB G) ASSAY
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LFX·June 9, 2014
COBAS 6000 UL COBAS E+ CORE FIX CONFIG
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFX·February 23, 2010
ADVIA CENTAUR RUBELLA G (RUB G) ASSAY
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LFX·February 22, 2010
AXSYM RUBELLA IGG
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LFX·February 18, 2010
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFX·March 10, 2010