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Catheterization kits recalled after 10 injuries, 1 death: FDA

Catheterization kits recalled after 10 injuries, 1 death: FDA
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FDA Announces Teleflex and Arrow International Recall of ARROW QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits for Increased Resistance That May Lead to Vessel Injuries, Narrowing, or Blockage

FDA Announces Teleflex and Arrow International Recall of ARROW QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits for Increased Resistance That May Lead to Vessel Injuries, Narrowing, or Blockage
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Drug administrationTeleflex arrow internationalAdverse event reporting programCustomer serviceTeleflex customer serviceArrow international customer serviceHarrow internationalFlash radial arteryArterial line catheterization kitsArterial line catheterizationRecall databaseMay be affectedUrgent medical device recallReturn goods authorizationTeleflex customer