ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 8
Summary
The FDA issued a Class I for ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 1 by Medinatura New Mexico, inc.. Reason: Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromob.
Details
Source
Drug Recall
External ID
D-0288-2026
Action Date
2026-01-14
Status
Ongoing
Category
drug
Product Description
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
Lot/Code Info: All lots within expiry.
Reason for Recall
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Distribution
Nationwide in the US
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-12
Company
Albuquerque, NM
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 36 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Medinatura New Mexico, inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Medinatura New Mexico, inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Medinatura New Mexico, inc. have FDA actions?
Medinatura New Mexico, inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0288-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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