FDA Recalls Infusion Pump and Tissue Stabilizer

Patrick Malone & Associates P.C. | DC Injury Lawyers
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The Food and Drug Administration has issued Class I recalls of Hospira Symbiq One and Two-Channel infusers and Medtronic Octopus Nuvo tissue stabilizers.

Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.

Please see full publication below for more information.

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