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.
Reported: October 1, 2014 Initiated: July 25, 2014 #Z-2670-2014
Product Description
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.
Reason for Recall
Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
Details
- Recalling Firm
- Centurion Medical Products Corporation
- Units Affected
- 21388
- Distribution
- 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.
- Location
- Williamston, MI
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Centurion Medical Products Corporation. Units affected: 21388.
Why was this product recalled? ▼
Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 1, 2014. Severity: Moderate. Recall number: Z-2670-2014.
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