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7733 — OLYMPUS News Story

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Brief: FDA Says Olympus Removes Endoscope Instrument Single Use Guide Sheath Kits

Feb 28 (Reuters) - FDA:

FDA:ENDOSCOPE INSTRUMENT RECALL, OLYMPUS REMOVES SINGLE USE GUIDE SHEATH KITS DUE TO RISK FOR RADIOPAQUE GUIDE SHEATH TIP DETACHING DURING PROCEDURES

FDA: IDENTIFIED OLYMPUS ENDOSCOPE INSTRUMENT RECALL AS MOST SERIOUS TYPE

FDA: 26 SERIOUS REPORTED INJURIES RELATED TO OLYMPUS ENDOSCOPE INSTRUMENT, SINGLE USE GUIDE SHEATH KITS

Source text: [ID:]

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