26 results · 12ms · Sources: EU EUDAMED, US FDA

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G-6-PDH Normal Control (G-6-PDH CONTROL N), Catalogue Number PD2618 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of Glucose-6-Phosphate Dehydrogenase in erythrocytes

FDA Recall
Terminated ·Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland·Product code JBL·April 3, 2019

G-6-PDH Deficient Control (G-6-PDH CONTROL D), Catalogue Number PD2617 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of Glucose-6-Phosphate Dehydrogenase in erythrocytes

FDA Recall
Terminated ·Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland·Product code JBL·April 3, 2019

BD Vacutainer Push Button Blood collection Sets with Pre-Attached Holder; Catalog Number: 368656; 23 g X12 " PBBCS w/PAH (Preattached), BD Diagnostics, Franklin Lakes, NJ

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·November 20, 2007

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

Lorad M-IV Mammography System

FDA Recall
Terminated ·Lorad, A Division of Hologic·Product code IZH·January 14, 2004

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

Lorad MIV Platinum Mammograpgy System

FDA Recall
Terminated ·Lorad, A Division of Hologic·Product code IZH·January 14, 2004

Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patients breast and the imaging receptor plate.

FDA Recall
Terminated ·Beekley Corporation·Product code IZH·July 2, 2012

Seneographe 2000D Digital Mammography X-Ray System

FDA Recall
Terminated ·General Electric Med Systems·Product code IZH·February 6, 2004

Diamond Mammographic X-Ray System, type MGX-2000, model 5111771. GE Healthcare P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.

FDA Recall
Terminated ·General Electric Med Systems LLC·Product code IZH·November 16, 2005

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

Seneographe DMR Mammography X-Ray System (all versions)

FDA Recall
Terminated ·General Electric Med Systems·Product code IZH·February 6, 2004

Hologic M-IV Mammography System; Model M4--00001. Intended to produce radiographic images of the breast. For screening and diagnostic imaging of the breast.

FDA Recall
Terminated ·Hologic, Inc.·Product code IZH·May 13, 2014

Seneographe 700T Mammography X-Ray Systems

FDA Recall
Terminated ·General Electric Med Systems·Product code IZH·February 6, 2004

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

GE Stereotaxy Positioner, model 2405544-2, for use with Senographe DS Full Field Mammography system, models 2383168, 2383168-2, 2383168-3, 2383168-3-1, 2383168-4-1. The expected use of the Senographe DS Stereotaxy is an optional accessory for the Senographe system for mammography examinations.

FDA Recall
Terminated ·GE Healthcare·Product code IZH·July 1, 2008