1,473 results
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21ms
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Sources: EU EUDAMED, US FDA
V-Probe, Endocare Cryo V Probe model # Cryo 206V. The product is used in a minimally invasive, percutaneous approach to treating prostate cancer in low, moderate and high risk patients. Prostate Cryoablation uses extremely cold temperatures to destroy cancerous tissue.
FDA Recall
Terminated
·Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.·Product code GEH·December 5, 2008
V-Probe, Endocare Cryo V Probe, single unit model # CVA2400. The product is used in a minimally invasive, percutaneous approach to treating prostate cancer in low, moderate and high risk patients. Prostate Cryoablation uses extremely cold temperatures to destroy cancerous tissue.
FDA Recall
Terminated
·Endocare, a Wholly Owned Subsidiary of HealthTronics, Inc.·Product code GEH·December 5, 2008
515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
515B Pulse Oximeter, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
515B Pulse Oximeter, RS232, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
French 100-120V 515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
Spanish 100-120V 515B Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
100-120V Oxypleth - 520A Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
100-120V Oxypleth - 520A Pulse Oximeter, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
Japanese 100-120V Oxypleth - 520A Pulse Oximeter- Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
Spanish 100-120V 2001 Pulse Oximeter WI - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
100-120V 2001 Pulse Oximeter With Mars - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
Span 100-120V 520A - OxyPleth Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
100-120V 515B with RS-232 Pulse Oximeter - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
100-120V 2001 Pulse Oximeter with Mars, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring.
FDA Recall
Terminated
·LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC·Product code MUU·August 8, 2017
100-120V 2001 Pulse Oximeter with Mars Nurse Call - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
100-120V 2001 Pulse Oximeter with Mars Nurse Call, Refurbished - Dixtal owned product. Intended use is to provide continuous, non-invasive monitoring of functional saturation (SpO2) and pulse rate.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code DQA·November 19, 2009
HSV 2 Primers, Catalog #18081020. Analyte Specific Reagent. The HSV-2 primer pair is specific for HSV-2 (Herpes Simplex Virus 2). For use in Clinical laboratories when developing their own diagnostic tests.
FDA Recall
Terminated
·Life Technologies Corporation·Product code NYQ·May 13, 2013
The product is a stainless steel stent mounted on a PTA balloon delivery device. The product is indicated for the palliation of malignant neoplasms in the biliary tree. The product is labeled as Edwards Lifesciences, LifeStent LP SDS, Biliary Endoprosthesis. Manufactured by ORBUS, MEDICAL TECHNOLOGIES. 5363 NW 35th Ave, Fort Lauderdale, FL, 33309. Ph 954 730-071, www. orbus.com. Distributed by: Edwards Lifesciences, Irvine, CA 82014-5888. Ref. Baloon-Expandable Stent and delivery System. Catalog Numbers SD186U14D SD186U24D SD366U14D SD366U24D
FDA Recall
Terminated
·Orbus Medical Technologies Inc·Product code MEW·March 19, 2004