American Health Packaging recalls 25 vials of Cyanocobalamin Injection (1000 mcg/mL) due to subpotent drug levels. This affects prescription-only medical use. Contact for details.
Subpotent Drug: Out of specification for assay.
American Health Packaging is recalling 25 vials of Cyanocobalamin Injection (1000 mcg/mL) because the drug concentration is too low. This could lead to ineffective treatment if used as prescribed.
The injection has lower-than-stated vitamin B12 levels, meaning it may not provide the intended medical benefit. This could result in treatment failure for patients needing the medication.
Prescription patients using this specific injection product. Healthcare providers who dispensed the recalled vials are most at risk.
Check for vials labeled 'Cyanocobalamin Injection, USP, 1000 mcg per mL, 25 x 1 mL Vials, Rx only'. The NDC for vial is 68001-509-59 and lots CCC210008 or CCC210009.
Verify the NDC code 68001-509-59 and lot numbers CCC210008 or CCC210009 on the vial.
The product may not provide the intended medical benefit due to low drug concentration, but it is not unsafe for immediate use.
Check for vials with NDC 68001-509-59 and lot numbers CCC210008 or CCC210009.
The recall does not specify a remedy, so contact American Health Packaging for guidance.
We’ve drafted a message you can send American Health Packaging to request your refund or repair — edit it as you like.
Subject: Recall D-0790-2022 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-0790-2022 from American Health Packaging. 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.
