Cardinal Health Recalls Monoject Saline Flush Syringes for Air Re-entry Risk

Serious injuries or death may result from the use of these devices. The FDA identified this as a Class I recall, the most serious type of re

If your email program has trouble displaying this email, view as a webpage. Cardinal Health Recalls Monoject Saline Flush Prefilled Syringes for Risk of Air Re-entering Syringe Leading to Air Embolism Cardinal Health is recalling the Monoject Saline Flush Prefilled Syringes because it is possible the syringe's plunger may allow air back into the syringe after the health care provider has pushed out (expelled) the air. This could result in injection of air into blood vessels and potential air embolism. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Read More Questions? If you have questions about this recall, contact the relevant Cardinal Health customer service group: Hospital customers: 800-964-5227 Federal government customers: 800-444-1166 Distributors: 800-635-6021 All other customers: 888-444-5440

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