Aurobindo Pharma recalls cyanocobalamin injection vials with subpotent drug levels. These injections may not contain enough active ingredient for effective treatment. Affected lots manufactured in India for specific expiration dates.
Subpotent Drug: Out of Specification results for Assay
Aurobindo Pharma is recalling cyanocobalamin (vitamin B12) injections that may have lower-than-stated drug levels. Using these injections could lead to ineffective treatment if the medication doesn't contain enough active ingredient.
The injections contain less active vitamin B12 than specified, meaning they might not provide the full therapeutic dose needed for treatment. This could result in ineffective treatment outcomes if the medication doesn't contain enough active ingredient.
Healthcare professionals who have received this specific cyanocobalamin injection vial for medical use. Patients receiving treatment with these vials may not get the full intended dose.
Check for vials labeled 'Cyanocobalamin Injection, USP, 1,000 mcg per mL, For IM or SC Use Only, 1 mL Vial, Rx Only' with the lot numbers CCC210004 through CCC210011. These were manufactured in India with specific expiration dates.
Look for the lot numbers CCC210004, CCC210005, CCC210006, CCC210007, CCC210010, or CCC210011 on the vial.
The recall is for potential subpotent drug levels, meaning the injections may not contain enough active ingredient for effective treatment. Using these vials could lead to ineffective treatment.
Check the vial label for the specific lot numbers mentioned in the recall. If you have the affected lots, contact your healthcare provider for guidance.
Look for vials with the lot numbers CCC210004 through CCC210011, manufactured in India with the specified expiration dates.
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0766-2022 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0766-2022 from Aurobindo Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
