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Olympus Recall Issued Over ShockPulse Device Miswiring: FDA
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Olympus Recall Issued Over ShockPulse Device Miswiring: FDA
Multiple recalls have been issued in recent years involving potentially defective Olympus medical device probes. Federal health officials are warning about problems with certain Olympus ShockPulseSE Lithotripsy System reusable probes after identifying a wiring defect that may delay treatment. The U.S. Food and Drug Administration (FDA) announced the Olympus S…
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