FDA recall, , High risk
BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse
Saline nasal spray may contain Aspergillus spp. and could cause serious infections in at-risk people.
Summary by Recall Canary from the FDA notice
What happened
Beekeeper's Naturals USA Inc., of Covina, California, is voluntarily recalling Beekeeper's Naturals Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, due to microbial contamination of non-sterile products. The recall, which began June 1, 2026, was announced June 11, 2026, and affects 1680 bottles distributed nationwide within the United States.
The product, sold only through Amazon, was produced at a third-party manufacturer and tested above acceptable levels. The recall was added to the FDA's Enforcement Report on June 9, 2026, and classified by the FDA on June 24, 2026.
What to do
If a code on your package is listed below:
- If you think you have this lot of Beekeeper’s Naturals Saline Nasal Spray.
- 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 regular mail or by fax.
Is yours affected?
Match the lot code and expiration date listed under your product.
Beekeeper's Naturals Saline Nasal Spray
- Lot code
- 5950
- Expiration date
- 02/2028
Recall details
- Company began the recall
- Sold in
Nationwide within the United States.
- Company
- BEEKEEPER'S NATURALS USA INC.Covina, California
- Hazard
- Contamination
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99145
- Recall number
- D-0620-2026
- Quantity recalled
- 1680 bottles
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
Announced by the company
In FDA's weekly enforcement report
Classified by FDA
Summary updated
