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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

... Read more »

Single Copies, Member Price: $300

ASA receives acknowledgement from OIG regarding request for Special Advisory Bulletin about the “company model”

April 29, 2009

ASA has received an acknowledgement of its March 19, 2009 letter to the Office of the Inspector General (OIG).  ASA had requested a Special Advisory Bulletin regarding the “company model.” 

Please use the following links to view copies of the letters.

ASA letter to OIG (March 19, 2009)
OIG acknowledgement (April 23, 2009)