13 results · 21ms · Sources: EU EUDAMED, US FDA

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ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 29, 2021

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 5, 2020

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·April 14, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH,INC.·Product code QJR·April 14, 2021

PROCLAIM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 1, 2017

SOLETRA

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 14, 2012

ARCHITECT IPTH

FDA Adverse Event
Malfunction ·ABBOTT GERMANY·Product code CEW·March 13, 2013

ASR ACETABULAR CUPS 48

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

UNK DEPUY FEMORAL COMPONENT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSA·February 20, 2008

ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE TIBIAL BUSHING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018

ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE FEMORAL BUSHING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018

ORTHOPEDIC SALVAGE SYSTEM LOCKING PIN

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018

ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018