ReBoost Nasal Spray recall
FDA recall D-0288-2026 · initiated Dec 12, 2025
Medinatura New Mexico, inc. recalled ReBoost Nasal Spray in Dec 2025 — an FDA Class I recall (D-0288-2026) because Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
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.
Sterility could not be assured
The maker could not guarantee the product was sterile. That matters most for injections and eye products, where a contaminated dose reaches past the body's defences.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
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
Frequently asked
- Was ReBoost Nasal Spray recalled?
- Medinatura New Mexico, inc. recalled ReBoost Nasal Spray in Dec 2025 — an FDA Class I recall (D-0288-2026) because Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. Most serious — a reasonable probability that use will cause serious harm or death.
- Why was ReBoost Nasal Spray recalled?
- Per the FDA enforcement record, the reason for recall D-0288-2026 was: Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
- Is a recalled ReBoost Nasal Spray dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of ReBoost Nasal Spray are affected?
- Distributed: Nationwide in the US. The recall covers these lots — All lots within expiry.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0288-2026.