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 MRP, LLC dba AMUSA Due to Incorrect expiration date on label
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 MRP, LLC dba AMUSA directly.
Affected Products
0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.
Quantity: 200,000 units
Why Was This Recalled?
Incorrect expiration date on label
Where Was This Sold?
This product was distributed to 6 states: AL, CT, IL, OH, PA, TN
About MRP, LLC dba AMUSA
MRP, LLC dba AMUSA has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report