Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes Recalled by Medefil Incorporated Due to The bar code that is printed on the...
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 Medefil Incorporated directly.
Affected Products
Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes, 100 units/mL, 3 mL fill in a 12 mL syringe.
Quantity: 1,608 Master Cartons
Why Was This Recalled?
The bar code that is printed on the Master Carton label does not correspond to the product code fully displayed on the Master Carton label. The non-matching information can only be detected by using a bar code reader. The defective bar codes will be read as Product No. MIH-3335 ( Heparin I.V. Flush Syringe 100 units/mL; 5 mL fill in 12 mL Syringe) whereas this product is actually Product No. MIH-3333 (Heparin I.V. Flush Syringe 100 units/mL; 3 mL fill in 12 mL Syringe).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medefil Incorporated
Medefil Incorporated has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report