9,997 results · 34ms · Sources: EU EUDAMED, US FDA

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FLEXISION BIOPSY NEEDLE

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC.·Product code EOQ·May 26, 2023

DUO FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 10, 2020

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·July 21, 2020

CADD MEDICATION CASSETTE RESERVOIR

FDA Adverse Event
Malfunction ·6000 NATHAN LN N·Product code FPA·August 21, 2024

MEDFUSION 4000 PUMP

FDA Adverse Event
Malfunction ·6000 NATHAN LN N·Product code FRN·August 20, 2024

CADD-SOLIS VIP PUMP

FDA Adverse Event
Malfunction ·6000 NATHAN LN N·Product code FRN·November 6, 2024

STELLAREX 0.035 OTW DRUG-COATED ANGIOPLASTY BALLOON

FDA Adverse Event
Injury ·PHILIPS IMAGE GUIDED THERAPY CORPORATION·Product code ONU·June 7, 2022

DUO FLUID CART - REFURBISHED

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·May 7, 2020

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·August 28, 2020

ZIMMER SKIN GRAFT MESHER

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·June 29, 2020

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FDA Adverse Event
UNK·Product code LNN·March 26, 2004

CORLINK AAD PROXIMAL

FDA Adverse Event
Other ·BYPASS MAAKAFIM LTD.·Product code LNN·October 1, 2003

CORLINK AAD PROXIMAL

FDA Adverse Event
Other ·BY-PASS MAAKAFIM LTD.·Product code LNN·October 1, 2003

CORLINK AAD PROXIMAL

FDA Adverse Event
Other ·BY-PASS MAAKAFIM LTD.·Product code LNN·October 1, 2003

NITINOL COMPRESSION ANASTOMOTIC DEVICE

FDA Adverse Event
Injury ·UNKNOWN·Product code LNN·March 28, 2013

BIODYNAMIX ANASTOMOSIS WITH COLONRING

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS·Product code LNN·December 30, 2009

VALTRAC

FDA Adverse Event
Malfunction ·DAVIS/GECK·Product code LNN·January 20, 1995

VALTRAC

FDA Adverse Event
Malfunction ·DAVIS/GECK·Product code LNN·January 18, 1995

VALTRAC ANASTOMOSIS RING

FDA Adverse Event
Injury ·DAVIS & GECK, INC.·Product code LNN·January 24, 1995

VALTRAC ANASTOMOSIS RING

FDA Adverse Event
Injury ·DAVIS AND GECK, INC.·Product code LNN·January 24, 1995