Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Ongoing Initiated Dec 12, 2025 (10 months ago)

ReBoost Nasal Spray

Class I — High risk. Reasonable probability of serious harm or death.

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.

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

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

Affected NDC 62795-4005-09

Compare with the code on your package — it is the most precise check available.

Category: Allergy & Cold Medication

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
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
NDC 62795-4005
SILVER NITRATE 10 [hp_X]/20mL; EUPHORBIA RESINIFERA RESIN 4 [hp_X]/20mL; CALCIUM SULFIDE 10 [hp_X]/20mL; GOLDENSEAL 5 [hp_X]/20mL; POTASSIUM DICHROMATE 6 [hp_X]/20mL; LUFFA OPERCULATA FRUIT 2 [hp_X]/20mL; SODIUM CARBONATE 6 [hp_X]/20mL; PULSATILLA VULGARIS 2 [hp_X]/20mL; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 20 [hp_X]/20mL; ECHINACEA, UNSPECIFIED 3 [hp_X]/20mL Spray
Nasal
MediNatura OTC
Recalling firm
Medinatura New Mexico, inc.
NDC code
62795-4005-9
Origin
NM, United States
Initiated by
Voluntary: Firm initiated
Company announcement
Dec 10, 2025 · FDA notice with lot numbers
FDA recall number
D-0288-2026 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week.

Other recalls by Medinatura New Mexico, inc.

All 2025 recalls
Class I · High risk

ClearLife Allergy Nasal Spray

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

Ongoing Microbial contamination Medinatura New Mexico, inc. NDC 62795-4006-9 D-0289-2026

Other microbial contamination recalls from 2025

All microbial contamination recalls
Class I · High risk

ClearLife Allergy Nasal Spray

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

Ongoing Microbial contamination Medinatura New Mexico, inc. NDC 62795-4006-9 D-0289-2026
Class I · High risk

Famotidine Injection

Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

Ongoing Microbial contamination Fresenius Kabi USA, LLC NDC 63323-739-11 D-0182-2026