Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection Recalled by Becton Dickinson & Company Due to BD received some reports of open seals found...
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
BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection, USP 10 mL REF 306553. Intended to be used only for the flushing of indwelling vascular access devices.10 mL BD PosiFlush Normal Saline Flush Syringes are generally compatible for use with syringe pumps.
Quantity: 3,088,320 units
Why Was This Recalled?
BD received some reports of open seals found on the BD Posiflush SF Flush Syringe 10 mL (Ref #306553).
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