Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
0.9% Sodium Chloride Injection Recalled by Centurion Medical Products Corporation Due to Unit packages may exhibit open seals which impacts...
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 Centurion Medical Products Corporation directly.
Affected Products
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion Convenience Kits. Recalled product is attached to the outside of the Convenience Kits.
Quantity: 21388
Why Was This Recalled?
Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
Where Was This Sold?
This product was distributed to 20 states: AZ, CA, IL, IN, IA, MD, MA, NE, NY, NC, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI
About Centurion Medical Products Corporation
Centurion Medical Products Corporation has 152 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report