119 results · 19ms · Sources: EU EUDAMED, US FDA

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Centurion brand sterile Huber needle infusion set, 20 GA x 1 inch; product EXHN010S.

FDA Recall
Terminated ·Tri-State Hospital Supply Corp·Product code KZH·March 8, 2005

Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or prevention of disease, or to affect the structure or any function of the body.

FDA Recall
Terminated ·International Medsurg Connection, Inc.·Product code KZH·June 23, 2017

Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm

FDA Recall
Terminated ·Arrow International Inc·Product code KZH·September 16, 2003

Cannon catheter hemodialysis catheterization set, 15 Fr x 36 cm

FDA Recall
Terminated ·Arrow International Inc·Product code KZH·September 16, 2003

1.0mL 28 G x 1/2" blister packaged insulin syringe Catalog Number 329424; Lot Number 0039920 Intended use: Subcutaneous injection of insulin.

FDA Recall
Terminated ·Becton Dickinson & Company·Product code KZH·June 15, 2011

Arrow central venous catheterization kit, 14 ga x 20 cm

FDA Recall
Terminated ·Arrow International Inc·Product code KZH·September 16, 2003

10 FR Super Arrow-Flex Percutaneous Sheath Introducer Set

FDA Recall
Terminated ·Arrow International Inc·Product code KZH·October 22, 2003

Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.

FDA Recall
Terminated ·Owen Mumford USA, Inc.·Product code KZH·November 24, 2014

Rocket KCH Fetal Bladder Drainage Catheter Model: R57405

FDA Recall
Terminated ·Rocket Medical Plc Industrial Estate Sedling Road Wear Indu Tyne & Wear Washington United Kingdom·Product code MPR·August 1, 2019

Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the demonstration of yeast and fungal elements in wet clinical preparations. Potassium Hydroxide digests the proteinaceous material in the specimen, leaving the fungal cell wall intact for direct microscopic observation.

FDA Recall
Terminated ·Gibson Bioscience·Product code JTO·July 1, 2021

Rocket KCH Fetal Bladder Drainage Catheter Model: R57405

FDA Enforcement
Class II ·Terminated·Rocket Medical Plc·December 4, 2019

Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the demonstration of yeast and fungal elements in wet clinical preparations. Potassium Hydroxide digests the proteinaceous material in the specimen, leaving the fungal cell wall intact for direct microscopic observation.

FDA Enforcement
Class II ·Terminated·Gibson Bioscience·September 22, 2021

Integra CUSA Excel Disposable Wrench. Catalog Number C5601. The CUSA Excel+ Sterile 23 kHz Torque Wrench is an accessory used with the CUSA Excel+ System ultrasonic surgical instrument. The torque wrench is used to properly secure the CUSA tip to the CUSA handpiece in the sterile field.

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·May 7, 2014

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 18, 2019