FDA Recall D-0289-2026

Medinatura New Mexico, inc. · Albuquerque, NM

Class I — life-threatening Ongoing 153 days on record

Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death. Distribution is nationwide and the recall remains in progress.

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

Lot / code: 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.

Recall record

Recall number: D-0289-2026
Classification: Class I
Status: Ongoing
Voluntary or mandated: Voluntary: Firm initiated
Firm notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution: Nationwide in the US
Recall initiated: 2025-12-12
Classified by FDA Center: 2026-01-15
FDA published: 2026-01-14
Recalling firm: Medinatura New Mexico, inc.
Firm location: Albuquerque, NM

Drug identification

Brand name(s): CLEARLIFE EXTRA STRENGTH
Generic name(s): ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED
Manufacturer(s): MediNatura Inc.
NDC(s): 62795-4006
Route(s): NASAL

Operational response

A Class I recall indicates a strong likelihood of serious adverse health consequence or death. Pull affected lots from active dispensing immediately. Segregate inventory in a marked, locked location pending destruction or return. If product has already been dispensed, identify affected patients and contact them by your standard recall-notification protocol.

For the official FDA enforcement record, see FDA's Recall Search.

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