532 results · 23ms · Sources: EU EUDAMED, US FDA

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SOMRYST

FDA Adverse Event
Injury ·PEAR THERAPEUTICS, INC.·Product code QVO·October 11, 2023

SCREW DVO DRIVE

FDA Adverse Event
Injury ·HOWMEDICA, INC.·Product code LRZ·December 2, 1992

COVERLOC VOLAR PLATE SHEATH, RADIAL, RIGHT

FDA Adverse Event
Malfunction ·DVO·Product code HRS·July 15, 2008

AVO CREAM TOPICAL EMULSION

FDA Adverse Event
Other ·Product code MGQ·September 16, 2014

OPTICATH CVO CATHETER EXPANDED KIT

FDA Adverse Event
Malfunction ·ICU MEDICAL,INC.·Product code FPA·March 27, 2014

DW ARTHROSCOPY FLUID MANAGEMENT DEV

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HRX·October 15, 2025

ONE PIECE MAIN PUMP&PATIENT EXT TBG

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HRX·October 28, 2025

CRYSTALENS

FDA Adverse Event
Injury ·EYEONICS, INC.·Product code HQL·October 17, 2006

VACUMAX

FDA Adverse Event
Death ·EVO MEDICAL SOLUTIONS·Product code BTA·May 4, 2010

EVO MEDICAL'S AEROMAX 3002 NEBULIZER

FDA Adverse Event
Malfunction ·EVO MEDICAL SOLUTIONS·Product code CAF·December 1, 2008

RAINDROP CORNEAL INLAY

FDA Adverse Event
Injury ·RVO 2.0, INC.·Product code LQE·May 23, 2024

MAXIASPIRATOR

FDA Adverse Event
Injury ·EVO MEDICAL SOLUTIONS·Product code BTI·September 4, 2012

RAINDROP INLAY

FDA Adverse Event
Injury ·RVO 2.0, INC.·Product code LQE·March 29, 2019

EVO MEDICAL'S AEROMAX 3002 NEBULIZER

FDA Adverse Event
Malfunction ·EVO MEDICAL SOLUTIONS·Product code CAF·March 3, 2008

RAIN DROP NEAR VISION INLAY

FDA Adverse Event
Malfunction ·RVO 2.0, INC·Product code LQE·December 19, 2019

CWIII ARTHROSCOPY PUMP

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code HRX·April 28, 2023

UNIVERSAL GLENOID CORRECTION REAMER

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·May 30, 2024

FLIPCUTTER II, SHORT 9.5MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HWE·May 20, 2024

SHAVER HP, APSII, HAND CONTROL

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HWE·May 7, 2024

ARTHREX ANGEL BMC KIT

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code ORG·June 12, 2024