71 results · 29ms · Sources: EU EUDAMED, US FDA

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Canon Aquilion Prime, Model TSX-303A

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion One, Model TSX-301A

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion Premium, Model TSX-301B

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion Precision, Model TSX-304A

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion Prime SP, Model TSX-303B

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion One Vision, Model TSX-301C

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion Lightning, Model TSX-036A

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

Canon Aquilion One, Model TSX-305A/3 V8.3 with FIRST 2.1

FDA Recall
Open, Classified ·Canon Medical System, USA, INC.·Product code JAK·March 25, 2019

INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453

FDA Recall
Terminated ·AAP Implantate Ag Lorenzweg 5 Berlin Germany·Product code HTW·January 25, 2019

INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425

FDA Recall
Terminated ·AAP Implantate Ag Lorenzweg 5 Berlin Germany·Product code HTW·January 25, 2019

AESCULAP TC COOELY MICRO NEEDLEHLDER SERR 200MM, product code MG524R. manual surgical instrument designed to grasp a suture needle

FDA Recall
Terminated ·Aesculap Implant Systems LLC·Product code HXK·September 25, 2019

myCordella Patient Kit without ECG, The Cordella System is a comprehensive at-home heart failure management platform that provides the clinician tools to monitor the progression of heart failure.

FDA Recall
Terminated ·ENDOTRONIX·Product code OUG·September 25, 2019

BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm, Total Length 112mm, Effective Length, 86mm - Product Usage: Twist drill intended use: to drill into bone in hip or knee surgeries.

FDA Recall
Terminated ·Brasseler USA I Lp·Product code GFF·October 18, 2019

SLIM Handle - catalogue #: SLM-HND100 a component of Simple Locking Intramedullary (SLIM) System

FDA Recall
Terminated ·Pega Medical Inc. 1111 Chomedey (A-13) E Laval Canada·Product code HSB·May 29, 2019

Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the endoscopes in between patient procedures.

FDA Recall
Terminated ·Medline Industries Inc·Product code MNL·April 25, 2019

K-Wire Single Trocar 1.6x150mm, Item Number OL15016S - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019

Go-EZ Screw 6.5x30, Item Number 19651 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019

Go-EZ Screw 6.5x32, Item Number 19652 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019

Go-EZ Screw 6.5x110, Item Number 19670 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019

K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine.

FDA Recall
Terminated ·BioPro, Inc.·Product code NBH·June 25, 2019