CLASS I ONGOING Drug recall · Reported 17 Jun 2026 · FDA Enforcement Report
Beekeeper's Naturals Saline Nasal Spray recalled
Beekeeper's Naturals USA is recalling Beekeeper's Naturals Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis +, distributed nationwide in the US. The recall was initiated on 1 Jun 2026 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0620-2026
- FDA event ID
- 99145
- Recalling firm
- Beekeeper's Naturals USA, Covina, CA
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 1 Jun 2026
- FDA classified
- 24 Jun 2026
- Reported
- 17 Jun 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Drug class
- Nasal Sprays
Timeline
| 1 Jun 2026 | Recall initiated by company | |
| 17 Jun 2026 | Published in enforcement report | +16 days |
| 24 Jun 2026 | Classified by FDA | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Non-Sterile Products
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
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.
Where it was distributed
Nationwide within the United States.
Questions about this recall
Why was it recalled?
Microbial Contamination of Non-Sterile Products
Which lots are affected?
Lot #: 5950, Exp. Date 02/2028
Where was it sold?
Nationwide within the United States.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.