ClearLife allergy nasal spray recalled over yeast, mold and microbial contamination
MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.
The agency’s classification
FDA (Drugs): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: Scored 5 because the FDA has classified this action as Class I, which the rubric maps directly to Critical.
Plain-English summary
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl oz (20 mL) bottles, distributed by MediNatura of Albuquerque, New Mexico, under NDC 62795-4006-9 and UPC 787647101887, is being recalled.
The reason given in the enforcement record is microbial contamination of non-sterile products: the products have been found to contain yeast and mold, and microbial contamination identified as Achromobacter.
The recall covers all lots within expiry. The record does not state a quantity. Distribution was nationwide in the US. The FDA has classified the action as Class I, its most serious category.
Consumers should stop using the product and follow the firm's instructions. Anyone who has used it and feels unwell should contact a healthcare provider.
The recalled product
- Product
- CLEARLIFE EXTRA STRENGTH (ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED)
- Brand
- CLEARLIFE EXTRA STRENGTH
- Manufacturer
- Medinatura New Mexico, inc.
- Category
- Drug — Nasal spray
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots within expiry.
UPCs (1)
- 787647101887
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Medinatura New Mexico, inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Medinatura New Mexico, inc.
See all →- CriticalReBoost nasal spray recalled over yeast, mold and microbial contamination
FDA (Drugs) · 2026-01-14
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