ZICAM COLD REMEDY MEDICATED NASAL SWABS recalled over sterility concerns
- Recall date
- June 6, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Church & Dwight Inc recalls ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewin…
- Recall number
- D-0504-2025
- FDA classification
- Class I
- Brand / firm
- Church & Dwight Inc
- Sold / distributed
- Nationwide in the USA.
Why it was recalled
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
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
ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
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