Fresenius has initiated a recall of 3 lots of 0.9% Sodium Chloride Injection USP, 1000 mL due to potential leakage of the parenteral/intravenous solution bag. Leakage of parenteral/intravenous solution bags may result in a breach of sterility, microbial contamination, or air embolism from air introduced to the IV system. If used in IV admixtures, there is potential for delivery of a more concentrated drug solution than intended. These lots were distributed in Canada between Jan 04, 2017 and April 28, 2017. Fresenius issued a recall notice on May 10, 2017.
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