PeriGiene recalled over sterility concerns
- Recall date
- July 17, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- DermaRite Industries, LLC recalls PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777…
- Recall number
- D-0613-2025
- FDA classification
- Class I
- Brand / firm
- DermaRite Industries, LLC
- Sold / distributed
- Nationwide within the USA
Why it was recalled
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08
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