Cyanocobalamin Injection — Class III drug recall D-0790-2022
Terminated recall by American Health Packaging, reported 2022-05-04, distributed in AL. Subpotent Drug: Out of specification for assay.
| Recall number | D-0790-2022 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Health Packaging, Columbus, OH, United States |
| Recall initiated | 2022-04-12 |
| Classified | 2022-04-26 |
| Reported by FDA | 2022-05-04 |
| Terminated | 2022-12-28 |
| Distributed | AL |
| Quantity | 97,975 vials |
| Reason classes | potency, specification failure |
| NDC | 68001-0509-59, 68001-0509-60 |
| Lot numbers | 01/23, CCC210008, CCC210009 |
Product
Cyanocobalamin Injection, USP, 1000 mcg per mL, For Intramuscular or Subcutaneous Use Only, 25 x 1 mL Vials, Rx only, Manufactured by: Eugia Pharma Specialties Limited, Hyderabad India for BluePoint Laboratories. NDC for Carton: 68001-509-60; NDC for vial: 68001-509-59
Reason for recall
Subpotent Drug: Out of specification for assay.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0790-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.