Codman—NEUROPATH Guiding Catheters: Packaging May Be Insufficient, Potentially Compromising Product Sterility

January 23, 2013 | Risk Management News

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ECRI Institute’s complete weekly summary of medical device hazard and recall information is available in ECRI Institute’s Health Devices Alerts(HDA). For more information about HDA, contact us at clientservices@ecri.org.

​In a January 11, 2013, Urgent Voluntary Product Recall Notification letter submitted by ECRI Institute member hospitals, Codman states that the packaging containing the guiding catheters below may be insufficient to withstand certain transportation methods, potentially resulting in damage to the sterile package and compromising product sterility. The manufacturer has not confirmed the...

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