HIGH

MediNatura Recalls ClearLife Allergy Nasal Spray for Contamination

MediNatura recalled ClearLife Allergy Nasal Spray on December 12, 2025, due to microbial contamination. The product contains yeast, mold, and Achromobacter. Consumers should stop use immediately and contact healthcare providers.

Quick Facts at a Glance

Recall Date
December 12, 2025
Hazard Level
HIGH
Brands
ClearLife Extra Strength, MediNatura
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Medinatura New Mexico, inc. or your healthcare provider for guidance. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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Product Details

The ClearLife Allergy Nasal Spray, Extra Strength, comes in 0.68 fl. oz. (20 mL) bottles. It is distributed by MediNatura, located at 10421 Research Rd., SE, Albuquerque, NM 87123. The product has a National Drug Code (NDC) of 62795-4006-9 and a UPC of 787647101887.

The Hazard

The nasal spray has been found to contain yeast, mold, and microbial contamination identified as Achromobacter. This contamination poses a high risk to consumers, particularly those with weakened immune systems.

Reported Incidents

There have been no reported injuries or deaths associated with this recall. However, the presence of Achromobacter can lead to serious infections, especially in vulnerable populations.

What to Do

Stop using the ClearLife Allergy Nasal Spray immediately. Contact MediNatura or your healthcare provider for guidance on next steps.

Contact Information

For more information, call MediNatura at the number provided on the product packaging. Additional details can be found at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0289-2026.

Key Facts

  • Product contains microbial contaminants
  • Stop use immediately
  • Contact healthcare provider for guidance
  • Distributed nationwide

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
All lots within expiry.
UPC Codes
62795-4006
62795-4006-9
7876471018
Affected States
ALL
Report Date
January 14, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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