Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Dodex Injectable (Cyanocobalamin Injection) USP Recalled by Accord Healthcare, Inc. Due to Subpotent drug: out of specification results
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 Accord Healthcare, Inc. directly.
Affected Products
Dodex Injectable (Cyanocobalamin Injection) USP, 1,000mcg/mL, 1mL multiple dose vial, Rx only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad-382 210, India, NDC 16729-533-08, UPC Code: 031672953308
Quantity: 52,998
Why Was This Recalled?
Subpotent drug: out of specification results
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Accord Healthcare, Inc.
Accord Healthcare, Inc. has 76 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report