107 results
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14ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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Route 92 Medical, Full Length 070 Reperfusion System, REF: 7001, Rxonly, SterileEO. Used for Introduction of interventional devices into the neurovasculature.
FDA Recall
Open, Classified
·Product code NRY·March 8, 2024
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspiration System including Cheetah Delivery Tool, REF: AP6072-132. 072 Aspiration Tubing, REF: APT-95
FDA Recall
Open, Classified
·Qapel Medical Inc.·Product code NRY·February 26, 2025
Trevo ProVue, Catalog: 90184
FDA Recall
Open, Classified
·Stryker Neurovascular·Product code NRY·April 23, 2024
Socrates 38 Aspiration Catheter 127 cm length REF SC038-127-001 The Socrates Aspiration System with a compatible suction pump is intended for use in the revascularization of patients with acute ischemic stroke
FDA Recall
Open, Classified
·Scientia Vascular, Inc.·Product code NRY·January 2, 2025
ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device designed to restore blood flow by effectively removing clots from occlusive vasculature in patients suffering from acute ischemic stroke.
FDA Recall
Open, Classified
·MICROVENTION INC.·Product code NRY·August 5, 2024
ARIES Extraction Kit; ARIES System; SYNCT , REF 50-10026, UDI # 00840487100073
FDA Recall
Open, Classified
·Luminex Corporation·Product code OOI·February 20, 2019
ARIES SARS-CoV-2 Assay
FDA Recall
Open, Classified
·Luminex Corporation·Product code QJR·July 14, 2022
Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452
FDA Recall
Open, Classified
·Luminex Corporation·Product code OZZ·February 20, 2019
ARIES SARS-CoV-2 Assay, REF: 50-10047
FDA Recall
Open, Classified
·Luminex Corporation·Product code QJR·September 14, 2022
ARIES GBS Assay , REF 50-10021, UDI # 00840487100165
FDA Recall
Open, Classified
·Luminex Corporation·Product code NJR·February 20, 2019
ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295
FDA Recall
Open, Classified
·Luminex Corporation·Product code PGI·February 20, 2019
ARIES C. difficile Assay , REF 50-10018, UDI # 00840487100059
FDA Recall
Open, Classified
·Luminex Corporation·Product code OZN·February 20, 2019
ARIES Group A Strep Assay , REF 50-10041, UDI # 00840487101469
FDA Recall
Open, Classified
·Luminex Corporation·Product code PGX·February 20, 2019
ARIES Flu A/B & RSV Assay , REF 50-10020, UDI # 00840487100158
FDA Recall
Open, Classified
·Luminex Corporation·Product code OZE·February 20, 2019
Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV4000-VZ
FDA Recall
Open, Classified
·Remel, Inc·Product code LRG·February 12, 2025
Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
FDA Recall
Open, Classified
·NRT X-RAY A/S Birkegardsvej 16 Hasselager Denmark·Product code OWB·April 17, 2024
Intelli-C, Left side suspended Tabletop, REF: 03400010
FDA Recall
Open, Classified
·NRT X-RAY A/S Birkegardsvej 16 Hasselager Denmark·Product code OWB·April 27, 2023
Intelli-C, Right side suspended Tabletop, REF: 03400000
FDA Recall
Open, Classified
·NRT X-RAY A/S Birkegardsvej 16 Hasselager Denmark·Product code OWB·April 27, 2023
1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
FDA Recall
Open, Classified
·NRT X-RAY A/S Birkegardsvej 16 BIRKEGAARDSVEJ 16 Hasselager Denmark·Product code OWB·January 21, 2022
BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9
FDA Recall
Open, Classified
·CareFusion 303, Inc.·Product code BRY·June 24, 2024