6 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code EZL·October 10, 2025
SURESTEP¿ FOLEY TRAY SYSTEM WITH BARD® LUBRI-SIL® CATHETER
FDA Adverse Event
Malfunction
·C. R. BARD, INC.·Product code EZL·September 12, 2022
BENDING/CUTTING PLIERS
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTC·June 12, 2020
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 3, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP·Product code LZG·December 21, 2010
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 17, 2014