Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe Recalled by Becton Dickinson & Company Due to An incorrect stopper was used in nine lots...
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 Becton Dickinson & Company directly.
Affected Products
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
Quantity: 5,085,120 units
Why Was This Recalled?
An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush Prefilled Flush Syringes with this stopper causes an increase in injection force, which has the potential to trigger alarms if used with a syringe pump.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Becton Dickinson & Company
Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report