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WEBINARS

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MEETINGS / EVENTS

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October 13 - 17 2012, 12:00 AM - 12:00 AM

ANESTHESIOLOGY 2012

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FDA MEDWATCH ALERTS

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May 16, 2012

Hydromorphone Hydrochloride Recall

Summary:

Hydromorphone Hydrochloride Recall

April 18, 2012

Morphine Sulfate Injection USP, 4 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject by Hospira, Inc: Recall - May Contain More Than Intended Fill Volume

Summary:

Customer report of two Carpujects syringes containing more than the 1 mL labeled fill volume. Opioid pain medications such as morphine have life-threatening consequences if overdosed. Those consequences can include respiratory depression (slowed breathing or suspension of breathing), and low blood pressure.

March 05, 2012

Cardiac Science Powerheart, CardioVive, CardioLife; GE Responder and Responder Pro; and Nihon-Kohden Automated External Defibrillators (AEDs): Class I Recall - Defective Component

Summary: FDA notified healthcare professionals and medical care organizations of the Class 1 recall of the listed AEDs which contain a component that may fail unexpectedly due to a defect. If the component were to fail during a rescue attempt, the AED may not deliver defibrillation therapy, causing serious adverse health consequences, including death. The unit’s self test may not detect the failure or impending failure of the component.

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ASA FEATURED PRODUCT

Anesthesiology Continuing Education (ACE) Program

SKU: 30702-12CE

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Single Copies, Member Price: $300

The Centers for Medicare and Medicaid Services (CMS) has issued a correction notice to the 2009 Physician Fee Schedule

January 02, 2009

The Centers for Medicare and Medicaid Services (CMS) has issued a correction notice to the 2009 Physician Fee Schedule. The 2009 schedule as published in November 2008 listed an incorrect global period of 90 days for CPT® codes:

63650 – Revision or removal of spinal neurostimulator electrode percutaneous array(s) or plate/paddle(s)
63685 – Insertion or replacement of spinal neurostimulator pulse generator or receive, direct or inductive coupling
63688 – Revision or removal of implanted spinal neurostimulator pulse generator or receiver

These codes will have a 10 day global period for services provided on/after January 1, 2009.  The notice appears in the December 31, 2008 Federal Register and is available at http://edocket.access.gpo.gov/2008/pdf/E8-31027.pdf