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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

DEA Schedules Fospropofol as Schedule IV Drug

Chicago — (October 6, 2009) 

The Drug Enforcement Administration (DEA) issued its final rule for the scheduling of fospropofol, which is effective November 5, 2009. In the final rule, the DEA placed fospropofol into schedule IV of the Controlled Substances Act, which means that the regulatory controls and criminal sanctions of Schedule IV will be applicable to the manufacture, distribution, dispensing, importation, and exportation of fospropofol and products containing fospropofol. Such scheduling will allow fospropofol to remain readily available for use by responsible clinicians in urgent and emergent situations, but will require that it be reasonably stored in a restricted and secure environment with access limited to qualified clinicians.

The ASA applauds this effort by the DEA and has fully supported the scheduling of fospropofol as a Schedule IV controlled substance. The DEA acknowledged the comments from ASA in its final rule stating that ASA “is in agreement with the findings of scientific and medical evaluation that formed the basis for the present rule controlling fospropofol as a schedule IV substant and [ASA] fully supported this control action.”

THE AMERICAN SOCIETY OF ANESTHESIOLOGISTS

Anesthesiologists: Physicians providing the lifeline of modern medicine. Founded in 1905, the American Society of Anesthesiologists is an educational, research and scientific association with 46,000 members organized to raise and maintain the standards of the medical practice of anesthesiology and improve the care of the patient.

For more information on the field of anesthesiology, visit the American Society of Anesthesiologists Web site at www.asahq.org. For patient information, visit LifeLineToModernMedicine.com

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Contact:

American Society of Anesthesiologists
communications@asahq.org
847-825-5586