176 results
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24ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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CINtec PLUS Cytology Kit (CE-IVD), Ventana Part Number 605-100, Roche GMMI 06889565001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
Hematoxylin II, Ventana Part Number 790-22087, Roche GMMI 05277965001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code HYJ·December 19, 2017
CINtec PLUS Cytology Kit (Canada/Japan), Ventana Part Number 805-100, Roche GMMI 06889549001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
ultraView SISH DNP Detection Kit US, Ventana Part Number 760-098, Roche GMMI 05572037001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code PPM·December 19, 2017
iView DAB IHC Detection Kit, Ventana part Number 760-091, Roche GMMI 05266157001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
OptiView Amplification Kit, Ventana Part Number 760-099, Roche GMMI 06396518001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
ultraView SISH Detection Kit, Ventana Part Number 780-001, Roche GMMI 05271967001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code PPM·December 19, 2017
NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Ventana Part Number 760-041, Roche GMMI 05266084001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
ultraView Universal DAB Detection Kit, Ventana part Number 760-500, Roche GMMI 05269806001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
OptiView Amplification Kit (250 Test), Ventana Part Number 860-099, Roche GMMI 06718663001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
ultraView SISH DNP Detection Kit, Ventana Part Number 800-098, Roche GMMI 05907136001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code PPM·December 19, 2017
OptiView DAB IHC Detection Kit, Ventana Part Number 760-700, Roche GMMI 06396500001 in vitro diagnostic
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code NJT·December 19, 2017
Tearaway Introducers, Catalog #: a) BNS-000-07, b) BNS-000-10; c) DIL-015-50; d) DSS-005-11; e) DSS-005-12; f) DSS-006-045; g) DSS-007-05; h) DSS-007-165; i) DSS-010-03; j) DSS-010-04; k) DSS-010-045; l) DSS-010-05; m) DSS-012-07; n) SPT-003-46
FDA Recall
Terminated
·Galt Medical Corporation·Product code DYB·May 2, 2018
smith&nephew EZCARE Negative Pressure Rx only. 100-240 V 12 V 50/60 Hz 90VA T1A 250 V Indicated for patients who would benefit from a suction device particularly as the device may promote healing when used with accessory wound sealing kits. Made in USA by/Fabrique aux Etals Unis par: Smith & Nephew, Inc., Largo, FL 33773 Smith & Nephew Medical Limited Hull HU3 2BN England
FDA Recall
Terminated
·Smith & Nephew Inc.·Product code OMP·January 29, 2010
Medicina Oral Tip Syringe 2.5ml Code: OT25
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022
Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022
Medicina Reusable Oral syringe 5ml Code: OTH05
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022
Medicina Oral Tip Syringe 1ml Code: OT01
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022
Medicina Reusable Oral syringe 1ml Code: OTH01
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022
Medicina Reusable Oral syringe 2.5ml Code: OTH25
FDA Recall
Open, Classified
·Medicina Uk Ltd·Product code KYW·July 4, 2022