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
Drug Recall
Official source record
- Recall number
- D-0288-2026
- Event ID
- 98095
- Classification
- Class I
- Status
- Ongoing
- Recalling company
- Medinatura New Mexico, inc.
- Reason for recall
- Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
- Report date
- January 14, 2026
- Recall initiation date
- December 12, 2025
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Nationwide in the US
Drug product identifiers
- Manufacturer
- MediNatura
- 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
- Substance names
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; CALCIUM SULFIDE; ECHINACEA, UNSPECIFIED; EUPHORBIA RESINIFERA RESIN; GOLDENSEAL; LUFFA OPERCULATA FRUIT; POTASSIUM DICHROMATE; PULSATILLA VULGARIS; SILVER NITRATE; SODIUM CARBONATE
- Product NDC
- 62795-4005
- Package NDCs
- 62795-4005-9; 7876471018
- Route
- NASAL
Where this information comes from
View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to the FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this medication?
Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.
Where can I find more official information?
The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.
