Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada Recalled by Becton Dickinson & Company Due to Limited number of syringes labeled Posiflush Experimental Product...
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 Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)
Quantity: 967,680
Why Was This Recalled?
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
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