467 results · 88ms · Sources: EU EUDAMED, US FDA

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ENDOSTAT ELECTROSURGICAL UNIT

FDA Adverse Event
Malfunction ·MEDICAL SCIENTIFIC, INC.·Product code KNS·June 25, 2007

ENDOSTATE 2

FDA Adverse Event
Other ·MEDICAL SCIENTIFIC, INC.·Product code GEI·July 8, 2004

ENDOSTAT ELECTROSURGICAL UNIT

FDA Adverse Event
Injury ·MEDICAL SCIENTIFIC, INC.·Product code KNS·November 22, 2006

ENDOSTAT ELECTROSURGICAL UNIT

FDA Adverse Event
Injury ·MEDICAL SCIENTIFIC, INC.·Product code KNS·November 22, 2006

Boston Scientific TSX Transseptal Needle, Model Number M004TSX60o; Used to create the primary puncture in the interatrial septum when passing an intruder and/or catheter through the septum from the right side of the heart to the left side.

FDA Enforcement
Class II ·Terminated·Merit Medical Systems, Inc.·April 20, 2016

PINNACLE PELVIC FLOOR REPAIR KITS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·November 20, 2010

GENERIC - CELSIUS THERMOCOOL TC

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·October 12, 2016

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·April 28, 2017

THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·May 15, 2018

Navilyst Medical, Inc. Vaxcel(TM) Port Titanium Standard Port with 8F Silicone Catheter (1.5 mm/2.6 mm), REF Catalog No. 45-320, UPN # - M001453200, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·January 18, 2019

Pointe Scientific Uric Acid (Liquid) Reagent Set, Pointe Scientific, Inc., Canton, MI; Catalog # HU782-246 and HU982-615. For the quantitative determination of uric acid in serum on Hitachi analyzers. For in-vitro diagnostic use only.

FDA Recall
Terminated ·Pointe Scientific, Inc.·Product code KNK·December 1, 2009

Pointe Scientific Liquid Uric Acid (R1) Reagent Set, Pointe Scientific, Inc., Canton, MI; Catalog # HU482-R1. For the quantitative determination of uric acid in serum on Hitachi analyzers. For in-vitro diagnostic use only.

FDA Recall
Terminated ·Pointe Scientific, Inc.·Product code KNK·December 1, 2009

Navilyst Medical, Inc., Vaxcel(TM) Port Titanium Mini-Port with 8F Silicone Catheter (1.5 mm/2.6 mm), REF Catalog No. 45-310, UPN Product No. M001453100, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

Navilyst Medical, Inc. Vaxcel(TM) Port titanium Mini-Port with 7F Polyurethane Catheter (1.3 mm/2.2 mm), REF Catalog No. 45-305, UPN Product No. M001453050, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

Navilyst Medical, Inc., Vaxcel(TM) Port Plastic Standard Port with 9F Polyurethane Catheter (1.8 mm/2.8 mm), REF Catalog No. 45-360, UPN Product No. M001453600, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

Navilyst Medical, Inc. Vaxcel(TM) Port titanium Standard Port with 9F Polyurethane Catheter (1.8 mm/2.8 mm), REF Catalog No. 45-315, UPN Product No. M001453150, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

Navilyst Medical, Inc. Vaxcel(TM) Port Titanium Mini-Port with 6F Polyurethane Catheter (1.1 mm/1.9 mm), REF Catalog No. 45-303, UPN Product No. M001453030, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

Navilyst Medical, Inc., Vaxcel(TM) Port Plastic Standard Port with 8F Silicone Catheter (1.5 mm/2.6 mm), REF Catalog No. 45-340, UPN Product No. M001453400, STERILE, Rx ONLY, For single use only --- Implantable Vascular Access System --- (kit contains Huber needle) -- previously distributed by Boston Scientific Corporation.

FDA Recall
Terminated ·Navilyst Medical, Inc·Product code LJT·May 13, 2010

ZIMMON BILIARY STENT

FDA Adverse Event
Injury ·COOK INC·Product code FGE·August 22, 2019