Latest Breaking News On - Arterial line catheterization kits - Page 1 : comparemela.com

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

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Increased resistance reported with some of the devices has led to 10 injuries and one death.

Drug administrationHarrow internationalArrow quickflash radial arteryArterial line catheterization kitsWatch safety informationAdverse event reporting

Latest Breaking News On - Arterial line catheterization kits - Page 1 : comparemela.com

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

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Increased resistance reported with some of the devices has led to 10 injuries and one death.Drug administrationHarrow internationalArrow quickflash radial arteryArterial line catheterization kitsWatch safety informationAdverse event reporting

Increased resistance reported with some of the devices has led to 10 injuries and one death.

Drug administrationHarrow internationalArrow quickflash radial arteryArterial line catheterization kitsWatch safety informationAdverse event reporting