Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard Access Systems Due to Some unit packages of BD PosiFlush SF Saline...
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 Bard Access Systems directly.
Affected Products
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Groshong Midline Bard MYPICC Kit 4F (Single-Lumen) The syringe is used to pre-flush the catheter prior to placement and may also be used to verify patency post-placement.
Quantity: 48 units
Why Was This Recalled?
Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit open seals, which could impact product sterility. Bard includes these pouched syringes, attached to some configurations of PICC kits, Port Access kits (PAK), PowerGlide kits, Midline kits, and Convenience kits.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Access Systems
Bard Access Systems has 24 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report