56 results
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21ms
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Sources: EU EUDAMED, US FDA
Access CEA Assay, Part No. 33200. For the quantitative determination of Carcinoembryonic Antigen (CEA) levels in human serum.
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code DHX·October 13, 2015
CEA / CD66e Ab-2, Product code RB-368-R7, RB-368-R1; 7 ml each. Description Carcinoembryonic antigen (CEA), is synthesized during development in the fetal gut, and is re-expressed in increased amounts in intestinal carcinomas and several other tumors. Antibody to CEA is reportedly useful in identifying the origin of various metastatic adenocarcinomas and in distinguishing pulmonary adenocarcinomas (60-70% are CEA+) from pleural mesotheliomas (rarely or weakly CEA+). This product is intended for qualitative immunohistochemistry with normal and neoplastic formalin-fixed, paraffin-embedded tissue sections, to be viewed by light microscopy.
FDA Recall
Terminated
·Lab Vision Corporation·Product code NJT·January 18, 2016
Access Immunoassay system CEA, in vitro diagnostic, Part No. 33200
FDA Recall
Terminated
·Beckman Coulter Inc·Product code DHX·April 12, 2006
IMMULITE /IMMULITE 1000 CEA
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code DHX·January 2, 2018
IMMULITE 2000/IMMULITE 2000 XPi CEA
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code DHX·January 2, 2018
Immulite 1000 CEA Catalog No. LKCE1
FDA Recall
Terminated
·Diagnostic Products Corp·Product code DHX·May 3, 2004
Germ Terminator, Toothbrush Steam Sterilization for Oral Health. Model GT100. The Germ Terminator uses steam heat to sanitize two manual toothbrushes or two toothbrush heads. Water is poured into a reservoir in the device's housing. The steam cycle is followed by a drying cycle.
FDA Recall
Terminated
·Ceg Enterprises Llc·Product code MCF·April 5, 2016
ST-AIA PACK CEA; Part Number: 025254 Assay, Tumor Marker
FDA Recall
Terminated
·Tosoh Bioscience Inc·Product code DHX·March 5, 2018
Immulite/ Immulite 1000 Carcinoembryonic Antigen (CEA) LKCE1 lot 302 and 303
FDA Recall
Terminated
·Diagnostic Products Corp·Product code DHX·May 26, 2005
CEA ELISA Kit. BioCheck, Foster City, CA 9440. Quantitative determination of AFP concentration in human serum.
FDA Recall
Terminated
·BioCheck Inc·Product code DHX·December 22, 2010
Vitros Immunodiagnostic Products CEA REAGENT PACK, Lot 750, REF 192 0115, 100 coated wells per pack. Firm on the label: Ortho-Clinical Diagnostics, Amersham, UK.
FDA Recall
Terminated
·Ortho-Clinical Diagnostics·Product code DHX·December 3, 2003
X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012
FDA Recall
Terminated
·X-Cel X-Ray Corp·Product code KPR--·November 12, 2002
Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JJE·June 29, 2018
Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JJE·June 29, 2018
Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JJE·June 29, 2018
Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JJE·June 29, 2018
Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JJE·June 29, 2018
Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code JJE·June 29, 2018
IMMULITE /IMMULITE 1000 Vitamin B12
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code CDD·January 2, 2018
IMMULITE /IMMULITE 1000 BR-MA (CA15-3)
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code MOI·January 2, 2018