Urgent Medical Device Recall: Monoject™ Flush Prefilled Syringes

Cardinal Health has issued a Medical Device Recall for specific catalog numbers of Monoject™ Flush Prefilled Syringes (0.9% Sodium Chloride) manufactured and distributed between July 2019 and July 2021 due to the potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe. This includes more than 260M units shipped to customers.

 

 

1. REVIEW your inventory for affected product.  
2. SEGREGATE and QUARANTINE all on-hand product per the Items Impacted table above.  
3. COMMUNICATE this notice to clinical staff through safety huddles to ensure awareness of this product issue.  
4. CONTACT your IMS Sales Representative or Customer Service to discuss next steps for product returns.