McKesson—Baxter Non-DEHP INTRAVIA Medication Delivery Bags: May Leak

​ECRI Institute's complete weekly summary of medical device hazard and recall information is available in ECRI Institute's Health Devices Alerts(HDA). For more information about HDA, contact us at clientservices@ecri.org.

Identify, isolate, and discontinue use of any affected product in your inventory. If you have affected product, verify that you have received the July 28, 2017, Urgent Drug Recall letter from McKesson or that you have been contacted by the manufacturer. Customers participating in a McKesson-administered Return to Vendor program should return affected product to their designated returns processor. Transmit a request for return authorization as unsaleable, manufacturer recall, using your McKesson Connect, Mobile Manager, or Telestock, and return affected product to McKesson. All others should follow the...