The Recall Desk
SevereFDA (Drugs)·D-0288-2026·Announced 2026-01-14

Nasal spray recalled for microbial and yeast contamination nationwide

ReBoost nasal spray is recalled nationwide due to contamination with yeast, mold, and Achromobacter bacteria. All lot numbers within expiration are affected.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class I classification requires a minimum score of 4 per the rubric. The product contains confirmed microbial contamination with no reported illnesses or injuries, placing it in the Severe range.

Plain-English summary

ReBoost nasal spray (0.68 fl. oz. bottles, NDC 62795-4005-9) is being recalled nationwide by Medinatura due to microbial contamination. The product contains yeast, mold, and the bacterium Achromobacter.

All lot numbers currently within expiration are affected by this recall, which applies to the entire United States. The manufacturer is Medinatura, located in Albuquerque, New Mexico.

Consumers who have purchased this product should discontinue use. Contact a healthcare provider if you have any health concerns after using this product.

The recalled product

Product
REBOOST (SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS)
Brand
REBOOST
Manufacturer
Medinatura New Mexico, inc.
Category
Drug — Nasal Spray
Hazard
  • microbial-contamination
  • achromobacter
  • yeast-mold

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)

  • 787647101863

Distribution

Distributed nationwide across the United States.

Related recalls

Same category