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Codman & Shurtleff, a division of Johnson & Johnson subsidiary DePuy Synthes, gets the FDA’s highest warning level for issues with certain lots of its programmable infusion pumps. The FDA puts its highest-risk label on a recall of programmable infusion pumps made by Codman &Shurtleff Inc., a division of Johnson & Johnson (NYSE:JNJ) subsidiary DePuy Orthopaedics. Codman’s implanted MedStream pumps were recalled over a potential defect in a component that measures the contents of the pump reservoir.
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