18 results
·
99ms
·
Sources: EU EUDAMED, US FDA
BELLAVISTA
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·June 23, 2025
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·May 29, 2018
TOSOH HLC-723G8 ANALYZER G8
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code LCP·August 2, 2018
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 16, 2010
VeinViewer (R) by Luminetx, Model Number VV1.0, Part No: P00399-L, Luminetx Corporation, Memphis, TN 38104 Product Usage: Non- invasive electronic visual aid device designed to project an image of a superficial subcutaneous vascular structures on the surface of the skin
FDA Recall
Terminated
·Christie Medical Holding Inc·Product code KZA·March 14, 2012
VeinViewer (R) by Luminetx, Model Number VV1.1 GS, Part No. P00800-L, Luminetx Corporation, Memphis, TN 38104 Product Usage: CTS Usage: Non- invasive electronic visual aid device designed to project an image of a superficial subcutaneous vascular structures on the surface of the skin
FDA Recall
Terminated
·Christie Medical Holding Inc·Product code KZA·March 14, 2012
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE·Product code ITI·September 1, 2011
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·March 30, 2017
CLEARTRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·August 7, 2013
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·April 5, 2017
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·July 18, 2017
STAR
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code LZS·July 18, 2017
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·March 23, 2017
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·June 20, 2017
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·June 20, 2017
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 14, 2010
System 1000 family of Hemodialysis Instruments, including the System 1000, Arena, 1550, BM11, BM25 and Meridian; Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A.
FDA Recall
Terminated
·Baxter Healthcare Renal Div·Product code FII·December 14, 2004
Advena Limited
Authorized representative
🇲🇹 Malta·467 Manufacturers·13717 Devices