Class II · Moderate risk Ongoing
[CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution
Reason Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
Hydrogen Peroxide 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
Hydrogen Peroxide Injection, all strengths and all presentations including Hydrogen Peroxide 3% 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-373-2013
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 Hydrogen recalls
See all
Class II · Moderate risk Ongoing
Hydrogen Peroxide Oral Rinse
Reason CGMP Deviations: products may not conform to the labeled specifications.
Class II · Moderate risk Ongoing
Colgate Anticavity Fluoride Toothpaste
Reason cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class II · Moderate risk Ongoing
Colgate Anticavity Fluoride Toothpaste
Reason cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class II · Moderate risk Terminated
Hydrogen Peroxide Topical Solution USP
Reason Cross Contamination With Other Products: Product is cross contaminated with low levels of isopropyl alcohol.
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