Class III · Low risk Ongoing
Levocarnitine Injection
Reason Labeling: Missing Label
Glutamine/Arginine/Carnitine 25 mg/100 mg/200 mg/mL 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
Glutamine/Arginine/Carnitine 25 mg/100 mg/200 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
- Recalling firm
- Wells Pharmacy Network LLC
- Origin
- FL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0359-2017
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
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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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