RecallRadar
FDA · DrugsClass I

Beekeeper's Naturals USA Inc. drug recall: BEEKEEPER'S NATURALS Saline Nasal Spray

Sterility concernsMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Drugs
Classification
Class I
Status
Ongoing
Event ID
99145
Recall initiated
Jun 1, 2026
Classified by FDA
Jun 24, 2026
Posted in Enforcement Report
Jun 17, 2026
Recalling firm
BEEKEEPER'S NATURALS USA INC.
Firm location
Covina, CA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Letter
Products in this event
1

What to do

Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.

View the official FDA record ↗

Reason for recall

Microbial Contamination of Non-Sterile Products

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jun 1, 2026. FDA classified it 23 days later, on Jun 24, 2026. Distribution reported by FDA: Nationwide within the United States.

Recalled products (1)

  • D-0620-2026 Class I Ongoing

    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.

    Codes / lots: Lot #: 5950, Exp. Date 02/2028

    Quantity: 1680 bottles

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA drug enforcement dataset
Official notice
FDA Enforcement Report, event 99145
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.