42 results
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11ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Maquet Getinge-BEQ-TOP 38300 ADULT CPS QID Material: 701055862
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019
Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019
Maquet Getinge-BEQ-TOP 25500 ECC 3/8 w/QiD Material: 701052461
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019
Maquet Getinge-BEQ-TOP 25503 TMC with BB & QiD Pedi Material:709000473
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019
BEQ-TOP 25500 ECC 3/8 w/QiD, Custom Tubing Kit, Catalog No. 701052461
FDA Recall
Terminated
·Datascope Corporation·Product code DTN·October 19, 2017
Maquet Getinge-BEQ-TOP 25500 ECC 3/8 w/QiD Material: 701052461
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·June 5, 2019
Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·June 5, 2019
Maquet Getinge-BEQ-TOP 25503 TMC ¿ with BB & QiD Pedi Material:709000473
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·June 5, 2019
MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number for the 50 count box is 57599-7400-4. The NDC number for the 100 count box is 57599-7401-5.
FDA Recall
Terminated
·AmeriSource Bergen·Product code CGA·January 30, 2004
BEQ-TOP 25500 ECC 3/8 w/QiD, Custom Tubing Kit, Catalog No. 701052461
FDA Enforcement
Class II
·Terminated·Datascope Corporation·May 16, 2018
Maquet Getinge-BEQ-TOP 38300 ADULT CPS QID Material: 701055862
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·June 5, 2019
Carestream DRX Evolution System (Standard Q) The DRX-Evolution System (Standard Q) is a permanently installed diagnostic x-ray system for generation of x-rays for examination of various anatomical regions. These products are permanently installed diagnostic x-ray systems composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary generator. In addition the device can use an x-ray table and /or wallstandbucky to complete x-ray exposures.
FDA Enforcement
Class II
·Terminated·Carestream Health Inc.·February 5, 2014
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)
FDA Recall
Terminated
·QiG Group LLC·Product code LGW·January 26, 2016
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel)
FDA Recall
Terminated
·QiG Group LLC·Product code LGW·January 26, 2016
Algostim LLC, Algovita External Pulse Generator, Trial Stimulator, Model 3400
FDA Recall
Terminated
·QiG Group LLC·Product code LGW·January 26, 2016
Velocity" Biopsy Valve, 25 units per box, Product Usage: The disposable Velocity biopsy valve is used to cover the opening of the biopsy inlet port of a flexible gastrointestinal endoscope. The Velocity biopsy valve provides access for endoscopic device passage and exchange, helps maintain insufflation, and minimizes leakage of biomaterial from the accessory port throughout the gastrointestinal endoscopic procedure. The Velocity biopsy valve provides a connection for irrigation through the Velocity irrigation pump.
FDA Recall
Terminated
·US Endoscopy Group Inc·Product code OCX·February 17, 2015
Duo-Flow IJ Full Tray; MCDLT114IJ MCDLT116IJ MCDLT118IJ
FDA Recall
Terminated
·Medical Components, Inc dba MedComp·Product code MPB·July 12, 2018
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2408 ( 3 x 8 channel)
FDA Enforcement
Class II
·Terminated·QiG Group LLC·March 30, 2016
Algostim LLC, Algovita External Pulse Generator, Trial Stimulator, Model 3400
FDA Enforcement
Class II
·Terminated·QiG Group LLC·March 30, 2016
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)
FDA Enforcement
Class II
·Terminated·QiG Group LLC·March 30, 2016