216 results · 22ms · Sources: EU EUDAMED, US FDA

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Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.

FDA Enforcement
Class II ·Terminated·Philips Electronics North America Corporation·February 17, 2016

Allura Xper FD OR Table, Ceiling version only; 722035; imaging applications.

FDA Enforcement
Class II ·Terminated·Philips Electronics North America Corporation·February 17, 2016

Universal Compact Head Ring Adapter Plate (UCHRAP), a component of the Universal Compact Head Ring Adapter, UCHRA. The UCHRA is a component of the Integra¿ CRW¿ Precision Arc Stereotactic System.

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·October 14, 2015

Leksell Vantage Stereotactic System. Instrument Carrier, Part of Leksell Vantage Arc (1053958). Neurological stereotaxic Instrument

FDA Enforcement
Class II ·Terminated·Elekta Inc·May 6, 2020

Milex Arcing Diaphragm Size 95; Model Number: MXWS95

FDA Enforcement
Class II ·Terminated·CooperSurgical, Inc.·March 16, 2016

Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.

FDA Recall
Terminated ·Philips Electronics North America Corporation·Product code OWB·November 3, 2015

Allura Xper FD OR Table, Ceiling version only; 722035; imaging applications.

FDA Recall
Terminated ·Philips Electronics North America Corporation·Product code OWB·November 3, 2015

Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf Collimator Model Number(s): product code: H54 and H56; MLC software version 8.5 - Product Usage: is intended to assist the clinician in the delivery of external beam radiation to defined target volumes during radiosurgery and radiotherapy while sparing surrounding normal tissue and critical organs from excess radiation.

FDA Enforcement
Class II ·Terminated·Varian Medical Systems, Inc.·May 13, 2020

ThermoFlo 1 HME, Disposable, Non-sterile, Expiry date 04/17. Used as a humidifier in a breathing circuit.

FDA Recall
Terminated ·Arc Medical Inc·Product code BYD·February 19, 2015

FOCAL Sim Workstation, Radiation Treatment Planning System. Used for patient contouring and viewing of treatment plan outputs. Also able to perform CT simulations and forward their information to the RTP System for dose calculation.

FDA Enforcement
Class II ·Terminated·Elekta, Inc.·September 10, 2014

Varian brand VARiS 1.4g (Medical Charged Particle Radiation Therapy System, Record and Verify System); Linear Accelerator with RTP Exchange v6.2, v6.6, & v8.0, All Models; Varian Medical Systems, Palo Alto, CA

FDA Recall
Terminated ·Varian Medical Systems Inc·Product code IYE·October 2, 2007

Milex Arcing Diaphragm Size 95; Model Number: MXWS95

FDA Recall
Terminated ·CooperSurgical, Inc.·Product code HDW·February 16, 2016

Monaco The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon and electron treatment plans and displays, on-screen and in hard-copy, two or three-dimensional radiation dose distributions inside patients for given treatment plan set-ups.

FDA Enforcement
Class II ·Terminated·Elekta, Inc.·September 10, 2014

Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA

FDA Enforcement
Class II ·Terminated·Omnilife Science Inc.·August 27, 2014

Apex ARC Hip Stem, HA Coated, Size 5; Product Code: HC-21005-HA Product Usage: The Apex ARC Hip Stem is the femoral component of a primary or revision total hip replacement. This femoral hip stem is intended for press-fit application and is provided sterile for single use. They are manufactured from titanium alloy. The stem has a proximal porous coating of titanium plasma spray under a coating of hydroxyapatite (HA)

FDA Enforcement
Class II ·Terminated·Omnilife Science Inc.·July 22, 2015

OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, REF ZBH-PSNCRCD39-L.

FDA Enforcement
Class II ·Terminated·Orthosensor, Inc.·October 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, REF ZBH-PSNCRCD39-R.

FDA Enforcement
Class II ·Terminated·Orthosensor, Inc.·October 17, 2018

Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA

FDA Recall
Terminated ·Omnilife Science Inc.·Product code LZO·May 9, 2014

Varian brand Trilogy System with RapidArc, Model Numbers: H14, H26, H27, H29; Distributed and Manufactured by: Varian Medical Systems Inc., Palo Alto, CA

FDA Recall
Terminated ·Varian Medical Systems Inc.·Product code IYE·July 20, 2010

Leksell Vantage Stereotactic System. Instrument Carrier, Part of Leksell Vantage Arc (1053958). Neurological stereotaxic Instrument

FDA Recall
Terminated ·Elekta Inc·Product code HAW·March 30, 2020