If you or someone in your household is in a higher-risk group—such as people with weakened immune systems or lung diseases—FDA says the affected product presents a reasonable probability that use could cause serious and life-threatening infections, including invasive sinusitis and lung infections.

What was recalled (check the lot code)

FDA says the recalled item is Beekeeper’s Naturals Saline Nasal Spray, sold in a single-unit 1 FL OZ (30 mL) bottle. The FDA notice says the lot number (5950) and expiration date (02/2028) are printed on the bottom or back label.

To identify the affected product, FDA instructs consumers to: check the lot number on the bottom or back label of your bottle. If it reads Lot 5950 (Best By: 02/2028), discontinue use.

FDA also states that no other Beekeeper’s Naturals products—including “Nasal Spray Max”—are impacted by this voluntary recall.

Why FDA is concerned

In its posting, FDA summarizes the company’s reason for the recall: the affected lot tested above acceptable microbiological limits for yeast and may contain Aspergillus spp.

FDA says the company has received four reports from customers regarding adverse reactions potentially related to the recalled product, including sinus congestion, irritation or infection.

Who should be most careful

FDA focuses its higher-risk language on “the population most at risk,” including people with weakened immune systems or lung diseases.

CDC notes that many people breathe in Aspergillus spores without getting sick. But CDC also explains that people with weakened immune systems or lung diseases are at higher risk for developing health problems due to Aspergillus, and that symptoms can range from mild to life-threatening.

CDC lists symptom examples by type, including for allergic Aspergillus sinusitis: stuffiness, runny nose, headache, and reduced ability to smell. For more severe forms such as invasive aspergillosis, CDC lists symptoms that can include fever, chest pain, cough, coughing up blood, and shortness of breath. CDC advises contacting a healthcare provider if you have symptoms you think are related to any form of aspergillosis.

What to do now if you have the spray

FDA’s immediate instructions are straightforward:

• Stop using lot #5950 (Best By: 02/2028).
• Contact Beekeeper’s Naturals at contact@beekeepersnaturals.com or 1-888-759-6910 (Monday–Friday, 8am to 8pm ET) for a refund, or if you have any other questions.
• If you have experienced any problems that may be related to taking or using this product, contact your physician or healthcare provider.

How to report possible side effects to FDA (MedWatch)

FDA says adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by

Sources

• FDA MedWatch: how to report adverse events
• CDC: Aspergillosis signs and symptoms