US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 29, 2023 (3 years ago)

Dodex Injectable Cyanocobalamin Injection, USP 1,000 mcg/mL, 25 x1 ML Multiple dose…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Sub-potent drug: assay test result below specifications at 9-month timepoint.

What was recalled

Dodex Injectable Cyanocobalamin Injection, USP 1,000 mcg/mL, 25 x1 ML Multiple dose vials, For Intramuscular or Subcutaneous Use Only, Rx Only, Sterile, Manufactured by: Intas Pharmaceuticals Limited Pharmaz Ahnedabad 382 213, INDIA, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-533-08.

Recalling firm
Accord Healthcare, Inc.
NDC code
16729-533-08
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0528-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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