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Unrated Drug recall · FDA · Published June 1, 2026

Beekeeper's Naturals Saline Nasal Spray Recall: Microbial Contamination Risk

Beekeeper's Natur: Saline nasal spray with propolis and xylitol recalled due to microbial contamination. No remedy specified in official notice.

🇺🇸 FDA recall #D-0620-2026DrugBeekeeper's Naturals ›
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Recalling firmBEEKEEPER'S NATURALS USA INC.440 N Barranca Ave # 9223 · Covina, CA 91723-1722
✎ GovInfoNow plain-language explainer

Beekeeper's Naturals is recalling saline nasal sprays that contain propolis and xylitol because they may have microbial contamination. This could pose a health risk if used improperly. Read more at govinfonow.com/recall/31246-beekeeper-s-naturals-saline-nasal-spray-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/31246-beekeeper-s-naturals-saline-nasal-spray-recall-microbial-contamination-risk · Updated August 10, 2026 · FDA enforcement record: FDA #D-0620-2026

Cite this page

“Beekeeper's Naturals Saline Nasal Spray Recall: Microbial Contamination Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/31246-beekeeper-s-naturals-saline-nasal-spray-recall-microbial-contamination-risk. Based on FDA recall #D-0620-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0620-2026%22&limit=1).

The FDA announced on June 1, 2026, that Beekeeper's Naturals USA Inc. is recalling BEEKEEPER'S NATURALS Saline Nasal Spray due to microbial contamination risks. The voluntary Class I recall affects 1,680 bottles distributed nationwide.

How to tell if you have it

  • Brand: Beekeeper's Naturals
  • Product: BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol
  • Size: 1 FL OZ (30 mL)
  • Lot #: 5950
  • Exp. Date: 02/2028

The hazard

The recall addresses microbial contamination of non-sterile products. The FDA classified the recall as Class I, indicating a situation where use could cause serious adverse health consequences or death.

Context

GovInfoNow's records show other recent recalls of similar products include Walgreens Saline Nasal Spray with Xylitol Recall (2025-11-12), Medinatura ReBoost Nasal Spray Recall (2025-12-12), and ClearLife Allergy Nasal Spray Recall (2025-12-12).

How to tell if you have this one

Check for bottles labeled 'Beekeeper's Naturals Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL)'. The lot number 5950 was manufactured for expiration date 02/2028.

  • Brand
    Beekeeper's Naturals
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name and lot number 5950 on the bottle label.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide within the United States.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 16 days after the firm started it.

1. Firm started the recall: Jun 1, 202612. Published in FDA’s Enforcement Report: Jun 17, 202623. FDA classified it Class I: Jun 24, 202632026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0620-2026 (June 1, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0620-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA