FDA DrugsClass I
ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 1...
Published: January 14, 2026Recall ID: D-0288-2026Category: drugsCountry: US
Reason for Recall / Hazard
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Product Description & Identification
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
Additional Source Details
| Field | Value |
|---|---|
| City | Albuquerque |
| State | NM |
| Openfda › Upc | 787647101863 |
| Openfda › Unii › 1 | RN2HC612GY |
| Openfda › Unii › 2 | 1MBW07J51Q |
| Openfda › Unii › 3 | 4N9P6CC1DX |
| Openfda › Unii › 4 | 1TI1O9028K |
| Openfda › Unii › 5 | ZW3Z11D0JV |
| Openfda › Unii › 6 | C4MO6809HU |
| Openfda › Unii › 7 | T4423S18FM |
| Openfda › Unii › 8 | I76KB35JEV |
| Openfda › Unii › 9 | 95IT3W8JZE |
| Openfda › Unii › 10 | 45P3261C7T |
| Openfda › Route | NASAL |
| Openfda › Spl id | dc9cb3f4-8286-48c3-bfa0-0ed53a3840b1 |
| Openfda › Brand name | REBOOST |
| Openfda › Spl set id | cb8a8d2a-d9d2-4a71-9279-c5641a9126c6 |
| Openfda › Package ndc › 1 | 62795-4005-9 |
| Openfda › Package ndc › 2 | 7876471018 |
| Openfda › Product ndc | 62795-4005 |
| Openfda › 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 |
| Openfda › Product type | HUMAN OTC DRUG |
| Openfda › Substance name › 1 | CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE |
| Openfda › Substance name › 2 | CALCIUM SULFIDE |
| Openfda › Substance name › 3 | ECHINACEA, UNSPECIFIED |
| Openfda › Substance name › 4 | EUPHORBIA RESINIFERA RESIN |
| Openfda › Substance name › 5 | GOLDENSEAL |
| Openfda › Substance name › 6 | LUFFA OPERCULATA FRUIT |
| Openfda › Substance name › 7 | POTASSIUM DICHROMATE |
| Openfda › Substance name › 8 | PULSATILLA VULGARIS |
| Openfda › Substance name › 9 | SILVER NITRATE |
| Openfda › Substance name › 10 | SODIUM CARBONATE |
| Openfda › Manufacturer name | MediNatura |
| Openfda › Is original packager | true |
| Event id | 98095 |
| Address 1 | 10421 Research Rd Se |
| Code info | All lots within expiry. |
| Postal code | 87123-3423 |
| Report date | 20260114 |
| Product type | Drugs |
| Reason for recall | Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251212 |
| Initial firm notification | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| Center classification date | 20260115 |
Overview
- Recalling FirmMedinatura New Mexico, inc.
- StatusOngoing
- Risk LevelClass I
- DistributionNationwide in the US