Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
23.4% Sodium Chloride Injection Recalled by The Ritedose Corporation Due to Labeling: Incorrect Barcode: Product barcode incorrectly identifies 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 The Ritedose Corporation directly.
Affected Products
23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx Only, RITEDOSE, 503B Outsourcing Facility, A Division of the RITEDOSE Corporation, 1 Technology Circle, Columbia, SC 29203, 1-866-994-4670, NDC: 65302-509-30, barcode N (01) 003 65302 50930 0
Quantity: 3795 syringes
Why Was This Recalled?
Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About The Ritedose Corporation
The Ritedose Corporation has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report