Recalls / Class I
Class ID-0289-2026
Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.
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
- Brand name
- Clearlife Extra Strength
- Generic name
- Onion, Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit, Sulfur, Ambrosia Artemisiifolia Whole, Euphrasia Stricta And Schoenocaulon Officinale Seed
- Active ingredients
- Ambrosia Artemisiifolia Whole, Euphrasia Stricta, Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit, Onion, Schoenocaulon Officinale Seed, Sulfur
- Route
- Nasal
- NDC
- 62795-4006
- Affected lot / code info
- All lots within expiry.
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.
Recalling firm
- Firm
- Medinatura New Mexico, inc.
- Manufacturer
- MediNatura Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 10421 Research Rd Se, Albuquerque, New Mexico 87123-3423
Distribution
- Distribution pattern
- Nationwide in the US
Timeline
- Recall initiated
- 2025-12-12
- FDA classified
- 2026-01-15
- Posted by FDA
- 2026-01-14
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0289-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.