Aug 23 (Reuters) - FDA:
* FDA: INARI MEDICAL UPDATES USE INSTRUCTIONS FOR
CLOTTRIEVER XL
CATHETER DUE TO REPORTS OF INJURY & DEATH FROM DEVICE
ENTRAPMENT, PULMONARY EMBOLI
* FDA: INARI MEDICAL'S RECALL INVOLVES UPDATING INSTRUCTIONS
FOR
CLOTTRIEVER XL, 30MM DEVICE, & AND IS NOT REMOVING THEM FROM
WHERE THEY ARE USED/SOLD
* FDA: IDENTIFIED INARI MEDICAL'S RECALL OF CLOTTRIEVER XL
CATHETER TO UPDATE INSTRUCTIONS AS THE MOST SERIOUS TYPE
* FDA: THERE HAVE BEEN 4 REPORTED INJURIES, 6 REPORTS OF
DEATH DUE
TO INARI MEDICAL'S CLOTTRIEVER XL CATHETER
((Reuters.Briefs@thomsonreuters.com;))