125 results
·
55ms
·
Sources: EU EUDAMED, US FDA
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 3, 2017
T:FLEX INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE·Product code LZG·March 23, 2017
SYNVISC ONE
FDA Adverse Event
Injury
·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020
SCULPTRA, POLY-L-LACTIC ACID
FDA Adverse Event
Injury
·VALEANT USA·Product code LMH·January 8, 2014
ETHISORB DURA PATCH
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GXQ·August 25, 2016
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·March 20, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·September 21, 2020
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 21, 2020
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 24, 2017
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·October 31, 2017
ELECSYS ACTH TEST SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CKG·November 21, 2016
CUSHING RONGEUR STR 2X10MM180MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code HTX·November 6, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·February 20, 2017
PDSII VIO 27IN 4-0 S/A SH-1
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code NEW·December 12, 2024
SYNVISC ONE
FDA Adverse Event
Injury
·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020
SYNVISC ONE
FDA Adverse Event
Injury
·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020
FLOSEAL
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - HAYWARD·Product code LMF·July 6, 2015
ACUVUE OASYS BRAND
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·March 25, 2014
SYNVISC ONE
FDA Adverse Event
Injury
·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020
Morph AccessPro Steerable Introducer; 6F Introducer, 45 cm working length Single use only. BioCardia, Inc. San Carlos, CA 94070 BioCardia Morph AccessPro is intended to provide a pathway through medical instruments cush as balloon dilation catheters, guidewires or other therapeutic devices that may be introduced into the peripheral vasculature.
FDA Recall
Terminated
·Biocardia, Inc.·Product code DYB·March 3, 2014