Expensive Medical Supplies Stolen From Hospitals

A medical supply rep from Maryland was recently charged in the theft of expensive medical kits from area hospitals that he later sold on eBay.  Each of the medical kits were sold for approximately $33,000 each, netting the man nearly $200,000. As this article from The Washington Post explains: “Burke Slater, 52, of Gaithersburg, was […]

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Medical Device Recalls Reach Historic Highs In 2018

The first quarter of 2018 included 343 medical device recalls by the US Food and Drug Administration (FDA). This was the highest for a first calendar quarter of any year on record and was up 126% from 2017. Experts point to the proliferation of software on medical devices as a primary driver for the record

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ASGE Releases New Infection Control Guidelines For Endoscopy

The American Society for Gastrointestinal Endoscopy recently released guidelines for infection control during GI endoscopy and related procedures. The guidelines come at a time when reports of endoscope-related infections are becoming more prevalent in the media. While the overall incidences of such infections are rarely reported, there is a strong possibility of underreporting of adverse

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FDA Issues Warning On Multi-Patient Endoscope Connectors

The U.S. Food and Drug Administration (FDA) recently released a public alert that warned about the risk of cross-contamination from the use of certain endoscope connectors commonly seen in gastrointestinal endoscopy. The alert primarily points out the risks associated with the use of 24-hour multi-patient use endoscope connectors that are labeled for use with multiple

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Hospitals Still Struggle To Combat Infectious Bacteria In Their Scopes

Recent research has once again shined the spotlight on the struggle hospitals face to rid their reusable medical endoscopes of dangerous bacteria. In this particular study, published in the American Journal of Infection Control, 71% of “patient-ready” scopes at 3 major US hospitals tested positive for bacteria. The study found problems in various types of

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How Supply Price Inaccuracies Can Affect The Bottom Line

Due to the nature of how hospitals and health systems acquire supplies, product prices are constantly changing. Different hospitals in the same health system, and even different departments within the same hospital, may be paying different rates for the same items, and those prices are typically in flux. With supply chains and individual departments within

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Supply Stock-Outs Have An Outsized Effect On The Bottom Line

A recent survey conducted by Cardinal Health showed that 40% of hospital staff have cancelled a case due to an out-of-stock supply, and 69% of staff have had to delay a case while a missing supply is being tracked down. Having spoken to hundreds of staff in operating rooms, cath labs and interventional radiology labs,

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Duodenoscope Surveillance Protocols Released By FDA and CDC

The U.S. Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDC) and American Society for Microbiology (ASM), along with other endoscope culturing experts, recently announced the availability of voluntary, standardized protocols that were developed for duodenoscope surveillance sampling and culturing. As noted by the FDA: “Hospitals and health care facilities that utilize

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Accreditation Firms Like Joint Commission Receive Further Scrutiny From Congress

Following the publication of a Wall Street Journal article last year, hospital accreditation organizations have received unwanted attention from the US Government. Members of the House Energy and Commerce Committee have requested additional information from the Centers for Medicare & Medicaid Services (CMS) and 4 major hospital accreditation organizations regarding their processes. Concerned with CMS’

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FDA Issues Warning To Duodenscope Manufacturers

Last week, the U.S. Food and Drug Administration (FDA) sent a warning to all three major duodenoscope manufacturers. The warnings were sent due to the failure of Olympus, Pentax and Fujifilm to comply with postmarket surveillance study requirements set with them by the FDA in 2015. During the FDA’s investigation of duodenoscope-related infections in 2015,

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