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FDA Recall of Monoject Saline Syringes

Rick

The FDA has announced a nationwide recall by Cardinal Health of their Select Monoject™ Prefilled Saline Syringes.


The affected syringes have been found to re-introduce air into the syringe after air has been expelled. 12 mL syringes filled with 3mL, 5mL, or 10mL, of saline have been affected.


For full details, consult your Cardinal Health supplier, Cardinal Health, or the FDA.

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The information contained herein is for educational purposes and for the benefit of licensed health care professionals. Much equipment in the dental office is under high pressure, carries high voltage electricity and/or can generate extreme temperatures.  Care should always be taken when performing repairs or maintenance. Under normal circumstances, equipment should be turned off, depressurized, and disconnected from power before performing service. It is the responsibility of the end-user to recognize and exercise appropriate caution.  All content copyright Dental-Techguru LLC.

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