192 results
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12ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Hospira brand Symbiq One-Channel Infuser; List Number: 16026; Distributed by: Hospira, Inc. Morgan Hill, CA and Manufactured by: Hospira Inc, La Aurora, Heredia, Costa Rica. Intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural or irrigation routes of administration.
FDA Recall
Terminated
·Hospira Inc·Product code FRN·April 9, 2010
RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical practitioners.
FDA Recall
Terminated
·Eizo Corporation 153 Shimokashiwano Hakusanshi Japan·Product code PGY·July 7, 2015
Hospira brand Symbiq Two-Channel Infuser; List Number: 16027; Distributed by: Hospira, Inc. Morgan Hill, CA and Manufactured by: Hospira Inc, La Aurora, Heredia, Costa Rica. Intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural or irrigation routes of administration.
FDA Recall
Terminated
·Hospira Inc·Product code FRN·April 9, 2010
InterGro DBM Demineralized Bone Matrix in a lipid carrier; Provided by: Lifelink Tissue Bank, Tampa, Florida, EBI A Biomet Company, Parsippany, New Jersey; REF DBM002. InterGro DBM product contain human tissue (allograft bpm) and are intended for transplantation. Products are to be used for filling bony voids or gaps in the extremities, and pelvis that are not intrinsic to the bony stability of the structure.
FDA Recall
Terminated
·Michigan Orthopaedic Products, Inc.·Product code MQV·May 5, 2008
"***BIOMET MICROFIXATION***CENTER DRIVE STAINLESS STEEL***2.0MM SYSTEM SCREWDRIVER BLADE***Non-Sterile Product***BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com***" Blade used to implant screws.
FDA Recall
Terminated
·Biomet Microfixation, Inc.·Product code LXH·March 15, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135417
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135615
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135715
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135512
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135612
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135412
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135720
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
Bard ConQuest PTA Balloon Dilatation Catheter, 12mm Balloon Size, Product Code: CQ-75124.
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·March 23, 2015
Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
FDA Recall
Terminated
·CareFusion 303, Inc.·Product code FPA·November 5, 2015
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135712
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135415
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135420
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135717
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135517
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010
BARD DORADO PTA BALLOON DILATATION CATHETERS, PRODUCT CODE # DR135520
FDA Recall
Terminated
·Bard Peripheral Vascular Inc·Product code DQY·May 4, 2010