16 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.

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL UM-D·Product code FPA·January 9, 2025

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·August 21, 2024

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL UM-D·Product code FPA·January 9, 2025

AUTOSOFT XC

FDA Adverse Event
Malfunction ·UNOMEDICAL UM-D·Product code FPA·January 9, 2025

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·January 6, 2025

GLENOSPHERE STANDARD OFFSET 40 MM DIAMETER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 9, 2022

CURLIN ADMINISTRATION SET

FDA Adverse Event
Malfunction ·MOOG MEDICAL·Product code FRN·February 12, 2013

AIR OPTIX TORIC

FDA Adverse Event
Injury ·PT CIBA VISION BATAM·Product code LPM·February 24, 2011

8010042-2008-00018

FDA Adverse Event
Malfunction ·Product code CBK·February 7, 2008

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·April 13, 2022

TRULIANT TIB IMP CR INS SLOPE++ SZ 4, 9MM

FDA Adverse Event
Injury ·EXACTECH INC.·Product code JWH·February 20, 2024

2.7X12MM HT X-DRIVE SCREW

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code HWC·August 4, 2016

2.7X8MM HT X-DRIVE SCREW

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code HWC·August 4, 2016

RETROFLEX3 INTRODUCER SHEATH

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYB·February 8, 2013

CR PROLONG 40MM BRNG +3 RET

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWS·February 9, 2022

OXF TWIN-PEG CMNTD FEM LG PMA

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·September 1, 2021