75 results · 74ms · 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.

BALLARD TURBO-CLEANING CLOSED SUCTION SYSTEM

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code BSY·February 19, 2025

TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

FDA Adverse Event
Injury ·MILLYARD ADVANCED MEDICAL PRODUCTS, LLC·Product code QFG·May 21, 2026

BALLARD CLOSED SUCTION SYSTEM

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code BSY·March 6, 2025

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·Product code FPA·August 11, 2021

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 5, 2021

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·Product code FPA·June 25, 2021

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·Product code FPA·July 8, 2021

HEALTHSMART PILL CRUSHER

FDA Adverse Event
Malfunction ·APOTHECARY PRODUCTS LLC.·Product code OHY·September 1, 2020

TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

FDA Adverse Event
Injury ·MILLYARD ADVANCED MEDICAL PRODUCTS, LLC·Product code QFG·March 31, 2026

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code LHI·March 30, 2021

TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

FDA Adverse Event
Injury ·MILLYARD ADVANCED MEDICAL PRODUCTS, LLC·Product code QFG·March 31, 2026

KNOTLESS PUSH-IN SUTURE ANCHOR

FDA Adverse Event
Malfunction ·PARCUS MEDICAL LLC·Product code MBI·June 12, 2023

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·Product code FPA·August 20, 2021

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 26, 2021

TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

FDA Adverse Event
Injury ·MILLYARD ADVANCED MEDICAL PRODUCTS, LLC·Product code QFG·April 2, 2026

UNKNOWN PARIETEX PRODUCT

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·August 11, 2023

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code LHI·March 8, 2021

SINGLE VIAL ACCESS DEVICE VENTED WITH SS

FDA Adverse Event
Malfunction ·Product code FPA·June 23, 2021

SMARTSITE 20MM VENTED VAD-MULTIPACK (25)

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code LHI·January 13, 2021

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·September 3, 2021