ReBoost Nasal Spray recalled over sterility concerns
- Recall date
- December 12, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Medinatura New Mexico, inc. recalls ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM…
- Recall number
- D-0288-2026
- FDA classification
- Class I
- Brand / firm
- Medinatura New Mexico, inc.
- Sold / distributed
- Nationwide in the US
Why it was recalled
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
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
ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863
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