Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Sep 29, 2023 (3 years ago)

Restore Sinus Spray

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Microbial contamination of Non-Sterile Products

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

Restore Sinus Spray, Manufactured by: Biomic Sciences, LLC Charlottesville, VA

Recalling firm
Biomic Sciences, LLC dba ION Intelligence of Nature
Origin
VA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0069-2024 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Biomic Sciences, LLC dba ION Intelligence of Nature

All 2023 recalls
Class I · High risk

ION*Sinus Spray

Microbial contamination of Non-Sterile Products

Terminated Microbial contamination Biomic Sciences, LLC dba ION Intelligence of Nature D-0067-2024

Other microbial contamination recalls from 2023

All microbial contamination recalls
Class II · Moderate risk

Premier Value Tussin Cough DM

CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.

Ongoing Microbial contamination Seaway Pharma Inc. D-0215-2024