FDAFDA · Food and drugs·Recall number 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
Published January 18, 2017 · Recall initiated: October 12, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling; Error on Declared Strength; product description incorrectly states HCG 7500 units instead of 5000 units. The primary panel is correct
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Pharm D Solutions, LLC
- Distributor
- AZ and WA
- Lot
- Lots: 07272016:03 Expiration Date: 01/23/2017 and 09142016:88 Expiration Date: 03/07/2017
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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