HIGH

MediNatura Recalls ReBoost Nasal Spray Due to Microbial Contamination

MediNatura recalled ReBoost Nasal Spray on December 12, 2025, due to microbial contamination. The affected product, distributed nationwide, contains yeast/mold and Achromobacter. Consumers should stop using the product immediately.

Quick Facts at a Glance

Recall Date
December 12, 2025
Hazard Level
HIGH
Brands
ReBoost, 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

ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, distributed by MediNatura. NDC 62795-4005-9, UPC 787647101863. Sold nationwide in the US.

The Hazard

The recall stems from microbial contamination, specifically the presence of yeast/mold and Achromobacter. These contaminants can pose serious health risks, especially for individuals with weakened immune systems.

Reported Incidents

No incidents or injuries have been reported related to this contamination as of the report date. The contamination risk is considered serious due to the potential health threats.

What to Do

Stop using ReBoost Nasal Spray immediately. Contact MediNatura or your healthcare provider for further guidance on the recall.

Contact Information

For more information, consumers can visit the FDA recall page or contact MediNatura directly at their Albuquerque, NM address.

Key Facts

  • Recall date: December 12, 2025
  • Report date: January 14, 2026
  • Class I recall due to serious health risks
  • Microbial contamination identified as Achromobacter
  • Distributed nationwide in the US

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
All lots within expiry.
UPC Codes
62795-4005
62795-4005-9
7876471018
Affected States
ALL
Report Date
January 14, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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