Medical Device Alert MDA/2008/051

July 21, 2008

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The MHRA have issued  a medical device alert (MDA/2008/051) which concerns the Kimal safety fistula needle. Kimal is aware of the potential for the unintentional retraction of the cannula into the protection sheath, which can result in exsanguination.  As a result, Kimal is recalling all lots of the device. 

 Click here to view the alert. 

 

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Written by IVTEAM · Filed Under All, IV Alert, IV News 

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