FDAFDA · Food and drugs·Recall number D-0923-2018
Glutathione 200mg/mL Injection w/Pres. (Benzyl Alcohol 1.5% in Sterile Water), 30 mL vial, Rx only, la VITA Compounding Pharmacy, 858.453.2500
Published July 25, 2018 · Recall initiated: June 25, 2018
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 Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- La Vita Compounding Pharmacy, LLC
- Distributor
- Product was distributed to patients via patient specific prescription only in CA.
- Lot
- Lot #: 144326@3, Exp 07/10/2018; 145953@2, Exp 08/05/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.