San Diego, CA, United States
La Vita Compounding Pharmacy, LLC recalls
1 recall recorded since 2018, most recently on 25 June 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Drugs
- Recall started
- 25 June 2018
- Terminated
- 18 January 2019
- Reason
- Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
- Distribution
- Product was distributed to patients via patient specific prescription only in CA.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- D-0922-2018, D-0921-2018, D-0923-2018
- Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharmacy, 858.453.2500
- Methylcobalamin 1mg/mL Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), packaged in 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharmacy, 858.453.2500
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.