Discussions in Infection Control

An independent site by Lawrence F Muscarella PhD -- a national authority on the causes and prevention of healthcare-associated infections and related errors.

Category: Device Recalls

510(k) Clearances Data Validation Duodenoscopes Echo-endoscopes Endoscopic Ultrasound (EUS) FUJIFILM ED-530XT Klebsiella pneumoniae carbapenemase]-producing K. pneumoniae Olympus TJF-Q180V OXA-48-producing Patty Murray (U.S. Senator) Pentax ED-3490TK Soluscope

The Redesigned Olympus Duodenoscope Has Been Linked to a ‘Superbug’ Cluster The device's original design was recalled in January 2016 amid concerns about its safety.

March 22, 2017 Lawrence F Muscarella PhD

March 21, 2017 (9:58 pm ET) — A “corrected” duodenoscope design introduced last year by the manufacturer to replace a recalled device has been linked to a “superbug” cluster, I…

CardioQuip Cincinnati Sub Zero Consent Decrees Data Validation Device Recalls Heater-Cooler Devices Informed Consent Legionella LivaNova (formerly Sorin Group) Maquet Medtronic Mycobacterium abscessus Mycobacterium chimaera Nontuberculous Mycobacteria ("NTM") Terumo

Infections Are Not Limited to the LivaNova’s Sorin 3T Heater-Cooler or to M. chimaera

January 18, 2017 Lawrence F Muscarella PhD

January 18, 2017 — More than one brand of a specialized type of medical equipment used during open-chest surgery has been linked to potentially life-threatening bacterial infections, my research has…

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