107 results · 21ms · Sources: EU EUDAMED, US FDA

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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