FDA Latest - Class I Medical Device Recall: Touchscreen for Hospira Symbiq Infusion System, Models 16026 and 16027

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Class I Medical Device Recall: Touchscreen for Hospira Symbiq Infusion System, Models 16026 and 16027

The Symbiq pump touchscreen may not respond to user selection, may experience a delayed response or may register a different value from the value selected by the user.

Source: Class I Medical Device Recall: Touchscreen for Hospira Symbiq Infusion System, Models 16026 and 16027