# FDA recall D-0427-2017

> **Pharm D Solutions, LLC** · Class III · drug recall initiated 2016-10-12.

## 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

## Distribution

AZ and WA

## Key facts

- **Recall number:** D-0427-2017
- **Recalling firm:** Pharm D Solutions, LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-10-12
- **Report date:** 2017-01-18
- **Termination date:** 2017-05-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0427-2017

## Citation

> AI Analytics. FDA recall D-0427-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0427-2017. Source: US FDA. Licensed CC0.

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