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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

2008 ASA Recommendations for Pre-Anesthesia Checkout

In 1993, a pre-anesthesia checkout recommendation was developed and widely accepted to be an important component of safe anesthesia practice. Since that time, new anesthesia delivery systems have been developed that require new checkout procedures. Further, new equipment designs are so different that a single checkout procedure is no longer applicable to them all. Updated recommendations have been developed over the last few years by a multi-disciplinary sub-committee of the ASA Committee on Equipment and Facilities including representatives of the American Society of Anesthesiologists, American Association of Nurse Anesthetists, American Academy of Anesthesiologist Assistants, and American Society of Anesthesia Technicians and Technologists. All of these professional organizations have also endorsed the final recommendations. The checkout design guideline is also supported as educational information by the Office of Device Evaluation, Food and Drug Administration.

The updated recommendations are intended to serve as general guidelines for individual departments and practitioners to design pre-anesthesia checkout procedures specific for the delivery systems and the needs of the local practice. A number of checkout procedures are also available that have been developed by individual departments using the design guideline and are tailored to specific anesthesia delivery systems. These sample checkout procedures are intended to serve as examples for other departments using similar equipment and facilitate developing their own checkout procedures. Both the general Recommendations and sample checkout procedures are available here for viewing and download by selecting the link below.

2008 Pre-Anesthesia Checkout Design Guidelines (View/Download)

Sample Pre-Anesthesia Checkout Procedures