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:] Further company coverage: 7733.T
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