Class II · Moderate risk Ongoing
Taurine for Injection
Reason Lack of Assurance of Sterility
Taurine Injection
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.
What was recalled
Taurine Injection, all strengths and all presentations including a) Taurine 50 mg/mL, b) Taurine-50-30 mL, c) Taurine-50 mg-30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
- Recalling firm
- FVS Holdings, Inc. dba. Green Valley Drugs
- Origin
- NV, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-411-2013
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 Taurine recalls
See all
Class II · Moderate risk Terminated
S-Taurine 50mg/Ml Mdv Soln
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
S-Calm Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Taurine 50 Mg/Ml
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Trim Calm
Reason Lack of sterility assurance.
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