80 results
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17ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.
FDA Recall
Open, Classified
·Integra LifeSciences Corp. (NeuroSciences)·Product code KTI·April 4, 2025
binx io CT/NG Assay- Single-use Cartridge for the qualitative detection of Chlamydia trachomatis and Neisseria gonorrhoeae Ref: 1.002.101
FDA Recall
Open, Classified
·Binx Health, Inc.
245 1st St Ste 18
Riverview II
Cambridge MA 02142-1292·Product code QEP·March 29, 2023
Beijing Syntech Laser APOLLO V+ Medical Platform surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser UL Station surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser Nice Station Light Based Platform surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser Trixel 11 C02 Laser surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser UL C02 Laser surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser Diode Laser surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser Trixel C02 Laser surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers
FDA Recall
Open, Classified
·Beijing Syntech Laser Co., Ltd International Industry Base West Area·Product code GEX·July 3, 2017
MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.
FDA Recall
Open, Classified
·Integra LifeSciences Corp. (NeuroSciences)·Product code FMF·May 23, 2025
CereLink ICP Monitor; Catalog No. 826820, 826820P. Intracranial pressure monitor.
FDA Recall
Open, Classified
·Integra LifeSciences Corp.·Product code GWM·June 22, 2022
VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly
FDA Recall
Open, Classified
·LivaNova USA Inc·Product code LYJ·November 16, 2018
BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
FDA Recall
Open, Classified
·CareFusion 303, Inc.·Product code FRN·May 21, 2024
CODMAN EVD BACTISEAL 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. Product Number: 821749
FDA Recall
Open, Classified
·Integra LifeSciences Corp.·Product code JXG·May 7, 2024
CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D. Catheter Set- indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. Product Number: 821750
FDA Recall
Open, Classified
·Integra LifeSciences Corp.·Product code JXG·May 7, 2024
CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. Product Number: 821745
FDA Recall
Open, Classified
·Integra LifeSciences Corp.·Product code JXG·May 7, 2024
Permobil TiLite, Models: Aero Z, and ZRA
FDA Recall
Open, Classified
·TiSport, Llc·Product code IOR·September 24, 2021
Ref No: HITHSP04 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
FDA Recall
Open, Classified
·Integra LifeSciences Corp.·Product code HBG·January 19, 2024
Ref No: HITHSP06 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
FDA Recall
Open, Classified
·Integra LifeSciences Corp.·Product code HBG·January 19, 2024