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Centurion Medical Products Corporation recalls 0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion Conveni
Recalled October 1, 2014 · FDA recall Z-2670-2014 · Centurion Medical Products
Hazard
Unit packages may exhibit open seals which impacts package integrity and potentially product sterility. · FDA Class II
Units
21388
Sold at
The product was distributed domestically to the following states: UT, WI, TX, NE, AZ, CA, IA, MD, NY, OK, PA, TN, TX, VA, NC, IL, MA, OR, WA, IN, SD.
Description
Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
Product
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.
Manufacturer(s)
Centurion Medical Products Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →