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 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…
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The Food and Drug Administration has issued an early alert for all heart pump controllers by Abiomed, which sent a correction notice to all customers with…
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The Food and Drug Administration has issued a Class I recall correction for certain Boston Scientific ACCOLADE pacemakers and cardiac resynchronization therapy…
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The Food and Drug Administration has identified a nationwide recall. Arrow International is recommending dialysis catheter kits containing Merit Medical 16F…
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h2, h3, h4 {color: #002855;} Postpartum hemorrhage (PPH) is one of the most common — and preventable — causes of maternal health in the United States. The…