10 results
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33ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Electrosurgical Tip Cleaner REF: 62-8499-001 Product Usage: electrosurgical accessory
FDA Recall
Terminated
·Xodus Medical Inc·Product code GEI·September 19, 2019
Electrosurgical Tip Cleaner REF: 138029 Product Usage: electrosurgical accessory
FDA Recall
Terminated
·Xodus Medical Inc·Product code GEI·September 19, 2019
Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory
FDA Recall
Terminated
·Xodus Medical Inc·Product code GEI·September 19, 2019
Electrosurgical Tip Cleaner REF: 62-8499-001 Product Usage: electrosurgical accessory
FDA Enforcement
Class II
·Terminated·Xodus Medical Inc·October 23, 2019
Electrosurgical Tip Cleaner REF: 138029 Product Usage: electrosurgical accessory
FDA Enforcement
Class II
·Terminated·Xodus Medical Inc·October 23, 2019
Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory
FDA Enforcement
Class II
·Terminated·Xodus Medical Inc·October 23, 2019
Exodus(TM) 10 F (3.4 mm)/ 35 cm Standard Loop Biliary Drainage Catheter with Hydrophilic Coating, REF/Catalog No. 10013, UPN/Product No. H965100131, STERILE --- Package/Box Units: Box of 5 eaches --- Made in USA: 2301 Centennial Blvd., Jeffersonville, IN 47130 -- Manufactured for: Navilyst Medical, Inc. 26 Forest Street, Marlborough, MA 01752 USA --- The Exodus Drainage Catheter consists of a radiopaque polyurethane catheter. The distal end of the catheter is configured as a J-Tip or a locking pigtail and is coated with a hydrophilic coating. Catheter markings are provided in centimeters on the shaft to indicate the distance from the distal tip. The Exodus Biliary Drainage Catheter includes a radiopaque (RO) marker band located approximate 5 mm from the most proximal drainage hole to assist with catheter placement. Biliary Drainage Catheters are intended for percutaneous drainage of the biliary tree.
FDA Recall
Terminated
·Navilyst Medical, Inc·Product code FGE·February 4, 2011
Exodus(TM) 8F (2.7 mm)/ 35 cm Standard Loop Biliary Drainage Catheter with Hydrophilic Coating, REF/ Catalog No. 10005, UPN/Product No. H965100051, STERILE --- Package/Box Units: Box of 5 eaches --- Made in USA: 2301 Centennial Blvd. Jeffersonville, IN 47130 -- Manufactured for: Navilyst Medical, Inc. 26 Forest Street Marlborough, MA 01752 --- The Exodus Drainage Catheter consists of a radiopaque polyurethane catheter. The distal end of the catheter is configured as a J-Tip or a locking pigtail and is coated with a hydrophilic coating. Catheter markings are provided in centimeters on the shaft to indicate the distance from the distal tip. The Exodus Biliary Drainage Catheter includes a radiopaque (RO) marker band located approximate 5 mm from the most proximal drainage hole to assist with catheter placement. Biliary Drainage Catheters are intended for percutaneous drainage of the biliary tree.
FDA Recall
Terminated
·Navilyst Medical, Inc·Product code FGE·February 4, 2011
Nonin Model 7600B cerebral oximeter pod. Used with the Nonin Model 7600 Regional Oximeter with Equanox Technology and Bluetooth Wireless Technology. Nonin Medical, Inc., 13700 First Avenue North, Plymouth, Minnesota 55441-5443 USA.
FDA Recall
Terminated
·Nonin Medical, Inc·Product code MUD·October 23, 2009
Exodus(TM) 8F (2.7 mm)/25 cm Standard Loop Multipurpose Drainage Catheter with Hydrophilic Coating, REF Catalog No. 10002, UPN Product No. H965100201, Rx ONLY, STERILE/EO --- Made in USA: 2301 Centennial Blvd., Jeffersonville, IN 47130 --- Manufactured for: Navilyst Medical, Inc. 26 Forest Street, Marlborough, MA 01752 USA --- Each box unit contains 5 catheters. --- The Exodus Standard Loop Multipurpose Drainage Catheter consists of a radiopaque polyurethane catheter with a locking pigtail distal end and is coated with a hydrophilic coating. Catheter markings are provided in centimeters on the shaft to indicate the distance form the distal tip. The catheter is provided with a trocar, a metal stiffening cannula and a plastic cannula. Multipurpose Drainage Catheters are intended for percutaneous drainage of fluid in the chest, abdomen and pelvis.
FDA Recall
Terminated
·Navilyst Medical, Inc·Product code FGE·May 24, 2010