124 results
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61ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FLUOREX®300
FDA UDI
G. T. LABORATORIES, INC.·B316FLX3000·Rigid-gas-permeable corrective contact lens, da...
FLUOREX®500UV
FDA UDI
G. T. LABORATORIES, INC.·B316FLX500UV0·Ridgid-gas-permeable corrective contact lens, d...
FLUOREX®700UV
FDA UDI
G. T. LABORATORIES, INC.·B316FLX700UV0·Ridgid-gas-permeable corrective contact lens, d...
FLUOREX®700
FDA UDI
G. T. LABORATORIES, INC.·B316FLX7000·Ridgid-gas-permeable corrective contact lens, d...
FLUOREX®300UV
FDA UDI
G. T. LABORATORIES, INC.·B316FLX300UV0·Ridgid-gas-permeable corrective contact lens, d...
FLUOREX®500
FDA UDI
G. T. LABORATORIES, INC.·B316FLX5000·Ridgid-gas-permeable corrective contact lens, d...
8031673-2017-00113
FDA Adverse Event
Malfunction
·November 17, 2017
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DYB·June 24, 2024
Genairex Securi-T Ostomy Deodorant (8 oz, 1 oz package sizes)
FDA Recall
Terminated
·BioMed Laboratories·Product code GDS·August 16, 2010
Reliamed Odor Eliminator Drops (8 oz, 4 oz, 1 oz package sizes)
FDA Recall
Terminated
·BioMed Laboratories·Product code GDS·August 16, 2010
Safen' simple Ostomy Appliance Deodorant (8 oz , 1 oz package sizes)
FDA Recall
Terminated
·BioMed Laboratories·Product code GDS·August 16, 2010
REFLEX ULTRA 45 COBLATOR II
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC., ENDOSCOPY DIVISION·Product code GEI·December 13, 2022
LAPRA-TY ABSORBABLE X6::SUTURE CLIP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code FZP·November 15, 2023
UNK_LASSO
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code DRF·September 15, 2020
COULTER AC-T 5diff Autoloader Hematology Analyzer, Part Number: 175356, Serial Numbers(s): All Serial Numbers The COULTER ACT-T 5diff Autoloader (AL) hematology analyzer is a 26-parameter, fully automated hematology analyzer, including a five-part leukocyte differential counter, capable of analyzing samples in a closed-vial Autoloader mode or a Manual (Stat) mode (open- or closed-vial).
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code GKZ·February 23, 2011
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code MMI·January 16, 2009
UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER.
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·May 22, 2011
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·July 17, 2011
LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098
FDA Recall
Terminated
·Magellan Diagnostics, Inc.·Product code DOF·May 7, 2021
LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004
FDA Recall
Terminated
·Magellan Diagnostics, Inc.·Product code DOF·May 7, 2021