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
USReBoost 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
Recalling Firm: Medinatura New Mexico, inc.
Grund für den Rückruf / Gefahr
TranslatedMicrobial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Produktbeschreibung & Identifikation
TranslatedReBoost 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 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, N...?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Übersicht
- Rückrufendes UnternehmenMedinatura New Mexico, inc.
- StatusOngoing
- RisikostufeClass I
- DistributionNationwide in the US
📢 Warnung teilen
Alert family and friends to keep them safe. Copy this quick alert message:
🚨 SAFETY ALERT: Medinatura New Mexico, inc. - 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 Check if your household is affected: https://therecallfile.com/de/recalls/reboost-nasal-spray-0-68-fl-oz-20-ml-bottles-distributed-by-medinatura/FDA-D-0288-2026
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