The Food and Drug Administration Feb. 18 announced that ICU Medical is voluntarily recalling certain lots of its potassium chloride injection bags with overwrap labels displaying 10 mEq that are packaged in 20 mEq cases. The FDA said the company learned of the issue from a customer complaint. The notice said the 20 mEq label printed on the bag is not visible or easily visible without manipulation when the 10 mEq overwrap is in place.

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The Food and Drug Administration has identified Class I recalls of two products: certain Astral ventilators by Resmed due to a supercapacitor that may leak…
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Baxter is voluntarily recalling a specific lot of intravenous solution due to a report of particulate matter in the solution identified as cardboard, according…
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The Food and Drug Administration has issued an early alert for specific lots of BD ChloraPrep Applicators by Medline because of a potential breach of sterility…
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The Food and Drug Administration has identified a Class I recall of North American Rescue first aid kits containing TRUE METRIX Blood Glucose Monitoring…
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The Food and Drug Administration has identified a Class I recall of reprocessed electrophysiology and ultrasound catheters by Medline Industries due…
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The Food and Drug Administration June 16 announced that a nationwide shortage of stereotactic breast biopsy needles is expected to last through the end of…