Pharm D Solutions HCG-Vitamin B12 5000 IU vial has strength error
Pharm D Solutions recalls HCG-Vitamin B12 vials with incorrect strength labeling. Product states 7500 units but should be 5000 units. No action needed as it's a labeling error.
Lower-risk recall
Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct
Contact the company
What happened, in plain English
Pharm D Solutions is recalling HCG-Vitamin B12 vials that incorrectly state 7500 units instead of 5000 units. This labeling error means the product might not be dosed correctly for medical use, but no action is required since it's a labeling issue. Read more at govinfonow.com/recall/42294-pharm-d-solutions-hcg-vitamin-b12-5000-iu-vial-has.
Source Summary by GovInfoNow · govinfonow.com/recall/42294-pharm-d-solutions-hcg-vitamin-b12-5000-iu-vial-has · Updated October 9, 2026 · FDA enforcement record: FDA #D-0427-2017
Cite this page
“Pharm D Solutions HCG-Vitamin B12 5000 IU vial has strength error.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42294-pharm-d-solutions-hcg-vitamin-b12-5000-iu-vial-has. Based on FDA recall #D-0427-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0427-2017%22&limit=1).
Why it’s dangerous
The product description incorrectly states HCG 7500 units instead of 5000 units. This labeling error could lead to incorrect dosing if the product is used without proper verification. However, the primary panel shows the correct strength.
Who’s affected
People who have the HCG-Vitamin B12 vials with the incorrect strength labeling. Medical users are most at risk due to potential dosing errors.
How to tell if you have this one
Check for vials labeled 'HCG-Vitamin B12 5000 IU-8 mg in 10 mL' with the incorrect strength. The vials were sold with specific lot numbers: 07272016:03 (expiring 01/23/2017) and 09142016:88 (expiring 03/07/2017).
- Brand
Pharm D Solutions- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
AZ and WA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0426-2017 | Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1709-04; Lot: 09122016:34, exp 09/07/2017 | 4 mL: 510 vials, 5 mL: 486 vials |
| D-0427-2017 | 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; Lots: 07272016:03 Expiration Date: 01/23/2017 and 09142016:88 Expiration Date: 03/07/2017 | 112 bottles |
What to do — step by step
Check Label
Verify the product description on the vial to confirm the strength is correctly labeled as 5000 units.
Where it went and when
Where it was distributed
Distributed in Arizona and Washington.
FDA distribution: “AZ and WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Washington.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #D-0427-2017 (October 12, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0427-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.