BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottl
Summary
The FDA issued a Class I for BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propo by BEEKEEPER'S NATURALS USA INC.. Reason: Microbial Contamination of Non-Sterile Products.
Details
Source
Drug Recall
External ID
D-0620-2026
Action Date
2026-06-17
Status
Ongoing
Category
drug
Product Description
BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91789.
Lot/Code Info: Lot #: 5950, Exp. Date 02/2028
Quantity Affected: 1680 bottles
Reason for Recall
Microbial Contamination of Non-Sterile Products
Distribution
Nationwide within the United States.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-01
Company
Covina, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 66 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (BEEKEEPER'S NATURALS USA INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does BEEKEEPER'S NATURALS USA INC. have FDA actions?
This is the only FDA action we have on record for BEEKEEPER'S NATURALS USA INC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0620-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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