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