FDAFDA · Food and drugs·Recall number D-0108-2023
QuadMix Super 002 (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine) 40mcg/30mg/4mg/0.4mg/mL INJECTABLE, packaged in 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
Published January 18, 2023 · Recall initiated: December 30, 2022
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
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Northern VA Compounders PLLC
- Distributor
- Nationwide in the USA
- Lot
- Lot#: 12062022@1, Exp 1/20/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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