HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial — Class III drug recall D-0427-2017
Terminated recall by Pharm D Solutions, LLC, reported 2017-01-18, distributed in AZ, WA. Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 un
| Recall number | D-0427-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharm D Solutions, LLC, Houston, TX, United States |
| Recall initiated | 2016-10-12 |
| Classified | 2017-01-09 |
| Reported by FDA | 2017-01-18 |
| Terminated | 2017-05-11 |
| Distributed | AZ, WA |
| Quantity | 112 bottles |
| Reason classes | labeling, potency |
| NDC | 69699-1723-20 |
| Expiration dates | 2017-01-23, 2017-03-07 |
Product
HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1723-20
Reason for recall
Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct
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-0427-2017. 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.