7 results · 8ms · Sources: EU EUDAMED, US FDA

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MEVION S250 Proton Radiation Treatment System; intended to deliver proton radiation treatment to patients

FDA Enforcement
Class II ·Terminated·Mevion Medical Systems, Inc.·July 29, 2020

MEVION S250i, MEVION S250; Proton Radiation Treatment System

FDA Enforcement
Class II ·Terminated·Mevion Medical Systems, Inc.·July 1, 2020

MEVION S250i, MEVION S250; Proton Radiation Treatment System - Product Usage: intended to deliver proton radiation treatment to patients with localized tumors or any other conditions susceptible to treatment by radiation

FDA Enforcement
Class II ·Terminated·Mevion Medical Systems, Inc.·December 2, 2020

LMA MADomizer, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce a straight stream instead of a fully atomized plume of medication. It is unlikely that serious adverse health consequences will occur in the event of a failure to deliver an atomized plume; however, this may result in inadequate topical anesthesia which may lead to some discomfort, further attempts to deliver topical anesthesia, or the use of alternative methods of anesthesia.

FDA Enforcement
Class II ·Terminated·Teleflex Medical·December 28, 2016

STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles.

FDA Enforcement
Class II ·Terminated·Advanced Sterilization Products·May 8, 2013

Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.

FDA Enforcement
Class II ·Terminated·Teleflex Medical·July 16, 2014

STERRAD Cyclesure Biological Indicator (BI), P/N 14324 are sold in cases, packaged as part of STERRAD System Validation kits and STERRAD test packs. The STERRAD CYCLESURE 24 Biological Indicator (BI), P/N 14324 is intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles.

FDA Enforcement
Class II ·Terminated·Advanced Sterilization Products·August 8, 2012