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 (US Distributed Catalog 306553) Recalled by Becton Dickinson & Company Due to This product has been confirmed to exhibit holes...
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 (US Distributed Catalog 306553), UDI 50382903065535
Quantity: 16,099,310 units
Why Was This Recalled?
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
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