360 results · 64ms · Sources: EU EUDAMED, US FDA

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U.S. TECHNOLOGIES, INC. RETRACTABLE SAFETY SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

ULTRA SAFE

FDA Adverse Event
Injury ·SAFETY SYRINGES INC.·Product code FMF·December 26, 2001

ULTRASAFE NEEDLE GUARD

FDA Adverse Event
Malfunction ·SAFETY SYRINGES, INC.·Product code FMI·December 4, 2002

B50 ULTRASAFE INJECTION SYSTEM NEEDLEGUARD

FDA Adverse Event
Other ·UNK·Product code FMF·September 22, 2001

UltraSafe Dental Needle Guard, P/N: 401801 Lot:T20201501

FDA Recall
Terminated ·Safety Syringes Inc·Product code MEG·September 5, 2002

NEEDLE 25G 1IN

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·November 26, 2024

VANISH POINT SYRINGE

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·April 27, 2021

VANISH POINT SYRINGE

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·April 27, 2021

VANISH POINT SYRINGE

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·April 27, 2021

VANISHPOINT

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·October 21, 2022

NEEDLE-PRO EDGE SAFETY DEVICE

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·February 22, 2011

CURAPLEX

FDA Adverse Event
Injury ·BOUND TREE MEDICAL, LLC·Product code CAE·February 28, 2020

VANISH POINT SYRINGE

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·April 27, 2021

SPINNING SPIROS CLOSED MALE LUER

FDA Adverse Event
Injury ·ICU MEDICAL INC.·Product code FPA·March 10, 2020

ASKU

FDA Adverse Event
Malfunction ·ASKU·Product code FMI·November 19, 2022

UNICEL® DXC 660I SYNCHRON® ACCESS® CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·September 9, 2010

VANISHPOINT SYRINGE

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·August 9, 2019

SYNCHRON® CX5CE CHEMISTRY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·September 9, 2010

COULTER® AC T 5DIFF CP ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GKZ·February 28, 2013

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code MEA·January 12, 2026