13 results · 24ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

MAGNUM INSTRUMENT

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·November 15, 2021

MAGNUM INSTRUMENT

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·February 15, 2023

MAGNUM INSTRUMENT

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·February 14, 2023

ENCOR ENSPIRE SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·March 4, 2023

MAGNUM INSTRUMENT

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·February 20, 2023

ENCOR DRIVER

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·March 4, 2023

SECURE 3 MED/SURG BEDOBS 01/13

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 21, 2013

ASR 300 SPIKED CUP SIZE 52

FDA Adverse Event
Injury ·DEPUY INTL. LTD.·Product code KWA·June 9, 2011

ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS) - PISTOL GRIP 36 CM - 15 MM ACT

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·August 14, 2008

ENCOR FOOT PEDAL

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·March 4, 2023

THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 6, 2018

QUICKSET ACE GRATER HEAD 63MM

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTO·May 22, 2024

MAGNUM INSTRUMENT

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 11, 2023