Hospira Issues A Voluntary Nationwide Recall Of Symbiq Infusion Systems Due To Inaccurate Response Of The Touch Screen To User Selection/Input

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Hospira Issues A Voluntary Nationwide Recall Of Symbiq Infusion Systems Due To Inaccurate Response Of The Touch Screen To User Selection/Input

10/29/2012 03:57 PM EDT

Hospira, Inc. (NYSE: HSP), announced today it is initiating a voluntary nationwide Class I recall of Symbiq™ infusion systems (list number 16026 Symbiq™ One-Channel Infuser and list number 16027 Symbiq™ Two-Channel Infuser, all serial numbers). This action is due to infusion pump LCD touch screens that may not respond to user selection, resulting in users possibly experiencing a delayed response and/or the screen registering a different value from the value selected by the user.

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