Class IOngoing

ReBoost Nasal Spray recall

FDA recall D-0288-2026 · initiated Dec 12, 2025

Most serious — a reasonable probability that use will cause serious harm or death.

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.

Details

Product: 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
Recalling company: Medinatura New Mexico, inc.
Classification: Class I
Status: Ongoing
Type: Voluntary: Firm initiated
Distribution: Nationwide in the US
Initiated: Dec 12, 2025
FDA report date: Jan 14, 2026

What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Source: openFDA Drug Enforcement record D-0288-2026 ↗

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