Nasal spray, 0.68 fl oz

• Product has been found to contain yeast/mold and microbial contamination with one species identified as Achromobacter, at levels above specifications.
• Company: MediNatura New Mexico Inc.
• Drugs
• FDA
• December 10, 2025

Product details

• Nasal spray, 0.68 fl oz

Company announcement

MediNatura New Mexico, Inc. is voluntarily recalling ReBoost Nasal Spray due to microbial contamination.

The product was distributed nationwide.

The recall was initiated December 10, 2025. No adverse events have been reported.

Risk:

There is a reasonable probability that adverse health consequences including life-threatening infections will occur with use of the product in the immuno-compromised population.

Impacted states: Nationwide

Products:

- ReBoost Nasal Spray (UPC code(s): 787647101863)

Contact

For more information, call (800) 621-7644 or email recall@medinatura.com.

View the original FDA notice

Browse all recalls

Related recalls

• 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container
• Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container
• 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container
• Thyroid Tablets, USP 30 mg
• Glutathione Injection 200MG/ML (30ML), Multi-Dose Vial
• Excel® Lactated Ringers Injection, 1000mL