Class II · Moderate risk Ongoing
L-Glutamine for Injection
Reason Lack of Assurance of Sterility
Glutamine 10 mg/mL Solution
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 10 mg/mL Solution, Pharm D Solutions, Houston, Texas ---- NDC 69699-1439-59
- Recalling firm
- Pharm D Solutions, LLC
- NDC code
- 69699-1439-59
- Origin
- TX, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0153-2019
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 Glutamine recalls
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Class II · Moderate risk Completed
Amino Blend Glutamine 30 mg/mL Ornithine HCL 50 mg/mL Arginine…
Reason Lack of assurance of sterility.
Class II · Moderate risk Ongoing
Goal
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
GAC (Glutamine/Arginine/L-Carnitine) 25mg/100mg/250mg/mL…
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Goal-Glutamine 75mg/Ornithine 75mg/Arginine 150mg/Lysine…
Reason Lack of assurance of sterility
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