1,668 results · 16ms · Sources: EU EUDAMED, US FDA

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Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm, Product Code 5-22512 2) EZ-ENDO 6.5 mm, Product Code 5-22513 3) EZ-ENDO 7.0 mm, Product Code 5-22514 4) EZ-ENDO 7.5 mm, Product Code 5-22515 5) EZ-ENDO 8.0 mm, Product Code 5-22516 6) EZ-ENDO 8.5 mm, Product Code 5-22517 Product Usage: Tracheal tube/airway management

FDA Enforcement
Class I ·Terminated·Teleflex Medical·June 26, 2019

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

FDA Enforcement
Class I ·Terminated·Nephron Pharmaceuticals Corp.·June 5, 2013

EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage.

FDA Enforcement
Class I ·Terminated·Nephron Pharmaceuticals Corp.·June 5, 2013

AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one (1) EZ Breathe Atomizer. For the delivery of liquid medications for respiratory usage.

FDA Enforcement
Class I ·Terminated·Nephron Pharmaceuticals Corp.·June 5, 2013

Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-22515 e) 8.0 mm, REF 5-22516 f) 8.5 mm, REF 5-22517 g) 9.0 mm, REF 5-22518 h) 6.0 mm, REF 5-22512 i) 6.5 mm, REF 5-22513 Product Usage: Tracheal tube/airway management

FDA Enforcement
Class I ·Terminated·Teleflex Medical·September 18, 2019

Ventstar Coax 180, MP03374

FDA Enforcement
Class I ·Terminated·Draeger Medical, Inc.·May 24, 2023

Anesthesia Circuit Kit Coax HEPA, MP17102

FDA Enforcement
Class I ·Terminated·Draeger Medical, Inc.·May 24, 2023

ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990-070U/ 7.0, 038-990-065U/ 6.5 *Note: product list updated per 12/23/2020 letter to customers

FDA Enforcement
Class I ·Terminated·Flexicare Medical Ltd.·December 2, 2020

Anesthesia Set Coax 180, MP03384

FDA Enforcement
Class I ·Terminated·Draeger Medical, Inc.·May 24, 2023

VentStar Watertrap (N) 180, MP00363

FDA Enforcement
Class I ·Terminated·Draeger Medical, Inc.·May 24, 2023

VentStar Bag Set (N) 110, MP00383

FDA Enforcement
Class I ·Terminated·Draeger Medical, Inc.·May 24, 2023

Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic

FDA Enforcement
Class I ·Terminated·Abbott Molecular, Inc.·October 20, 2021

Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fistulae and synthetic dialysis grafts.

FDA Enforcement
Class I ·Terminated·TELEFLEX MEDICAL INC·February 23, 2022

Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02

FDA Enforcement
Class I ·Terminated·CELLTRION USA INC·May 4, 2022

Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02

FDA Enforcement
Class I ·Terminated·CELLTRION USA INC·March 9, 2022

EXCOR Pediatric Ventricular Assist Device Blood Pumps, Models: P10P-001 (10 ml blood pump); P15P-001 (10 ml blood pump); P25P-001x01 (25 ml blood pump); P30P-001x01 (30 ml blood pump), P50P-001 (50 ml blood pump); P60P-001 (60 ml blood pump). Recall occurred in 2018, and was retrospectively reported.

FDA Enforcement
Class I ·Terminated·BERLIN HEART GMBH·May 31, 2023

Alaris System PC Unit Model 8015, a modular infusion pump and monitoring system

FDA Enforcement
Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020

NC TREK Coronary Dilatation Catheter, REF 1012455-08 Rx Only, NC TREK RX 5.00 X 8MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion b) balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction c) balloon dilatation of a stent after implantation (balloon models 2.00 mm 5.00 mm only)

FDA Enforcement
Class I ·Terminated·Abbott Vascular·February 26, 2020

NC TREK Coronary Dilatation Catheter, REF 1012453-20 Rx Only, NC TREK RX 4.00 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion b) balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction c) balloon dilatation of a stent after implantation (balloon models 2.00 mm 5.00 mm only)

FDA Enforcement
Class I ·Terminated·Abbott Vascular·February 26, 2020

Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿

FDA Enforcement
Class I ·Terminated·Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company·February 13, 2019