Class III · Low risk Ongoing
Levocarnitine Injection
Reason Labeling: Missing Label
L-Carnitine 250mg/Ml Inj Injectable
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of assurance of sterility
What was recalled
L-CARNITINE 250MG/ML INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
- Recalling firm
- Vita Pharmacy, LLC dba Talon Compounding Pharmacy
- Origin
- TX, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0122-2022
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Carnitine recalls
See all
Class II · Moderate risk Ongoing
Lipo MIC + L-Carnitine for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
L-Carnitine for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
LX Bioboost Plus
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Levocarnitine Oral Solution
Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.
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