Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial Recalled by Pharm D Solutions, LLC Due to Labeling; Error on Declared Strength; product description incorrectly...

Date: October 12, 2016
Company: Pharm D Solutions, LLC
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Pharm D Solutions, LLC directly.

Affected Products

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

Quantity: 112 bottles

Why Was This Recalled?

Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct

Where Was This Sold?

This product was distributed to 2 states: AZ, WA

Affected (2 states)Not affected

About Pharm D Solutions, LLC

Pharm D Solutions, LLC has 100 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report