FDA MedWatch - Advanced Sterilization Products (ASP) Sterrad Cyclesure 24 Biological Indicator: Safety Communication – Potential Risk of Infection

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Title: FDA MedWatch - Advanced Sterilization Products (ASP) Sterrad Cyclesure 24 Biological Indicator: Safety Communication - Potential Risk of Infection
MedWatch logoMedWatch - The FDA Safety Information and Adverse Event Reporting Program

Advanced Sterilization Products (ASP) Sterrad Cyclesure 24 Biological Indicator: Safety Communication – Potential Risk of Infection

AUDIENCE: Risk Manager, Surgery, Infectious Disease

ISSUE: An FDA review of ASP data showed that the Sterrad Cyclesure 24 Biological Indicators cannot effectively monitor the sterilization process throughout the indicated 15-month shelf life.  After reviewing additional ASP data, the FDA believes that the product may be used with a 6-month shelf life. 

BACKGROUND: The Sterrad Cyclesure 24 Biological Indicator is a product used periodically to monitor and confirm the microbicidal effectiveness of the sterilization process in Sterrad sterilizers.  A biological indicator is used, in conjunction with other methods, to monitor sterilization systems.

Sterrad sterilizers are used for devices that must be sterilized at low temperatures, such as multiple single-channel flexible endoscopes, cameras, some rigid scopes, light cords, batteries, and power drills.

ASP’s Sterrad Cyclesure 24 Biological Indicator is the only biological indicator that can be used with the Sterrad sterilizer.  Biological indicators from other manufacturers are not designed for this use and have not been cleared by the Food and Drug Administration (FDA) for use in Sterrad sterilizers.

RECOMMENDATIONS:

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

Please include the following information in your reports, if available:

Read the FDA Safety Communication at:

http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm310549.htm


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