Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due to Potential for the plunger to draw back after...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cardinal Health directly.
Affected Products
Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
Quantity: 267,217,860 eaches in total
Why Was This Recalled?
Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cardinal Health
Cardinal Health has 75 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report