FDA Drugs recall ·
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0289-2026
- Date
- (initiated December 12, 2025)
- Company / brand
- Medinatura New Mexico, inc.
10421 Research Rd Se, Albuquerque, NM, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Hazard tags
- Mold Sterility Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887
Why was it recalled?
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All lots within expiry.
Distribution
Nationwide in the US
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0289-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.