Recalls / Class I
Class ID-0288-2026
Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.
Product
ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863
- Brand name
- Reboost
- Generic name
- 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
- Active ingredients
- Cairina Moschata Heart/liver Autolysate, Calcium Sulfide, Echinacea, Unspecified, Euphorbia Resinifera Resin, Goldenseal, Luffa Operculata Fruit, Potassium Dichromate, Pulsatilla Vulgaris, Silver Nitrate, Sodium Carbonate
- Route
- Nasal
- NDC
- 62795-4005
- Affected lot / code info
- All lots within expiry.
Why it was recalled
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Recalling firm
- Firm
- Medinatura New Mexico, inc.
- Manufacturer
- MediNatura
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 10421 Research Rd Se, Albuquerque, New Mexico 87123-3423
Distribution
- Distribution pattern
- Nationwide in the US
Timeline
- Recall initiated
- 2025-12-12
- FDA classified
- 2026-01-15
- Posted by FDA
- 2026-01-14
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0288-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.