Stop using now Drug recall · FDA · Published December 17, 2020

ManukaGuard Nasal Spray Recall: Yeast Contamination Risk

NDAL Mfg Inc. recalls ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray due to yeast contamination. Check your lot number and expiration date.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0269-2021Drug ManukaGuard ›

Stop using this now

Microbial Contamination of Non-Sterile Products: Product confirmed to have yeast

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Contact the company

Recalling firmNDAL Mfg Inc.23745 Spectacular Bid Ln · Monterey, CA 93940-6527

✎ GovInfoNow plain-language explainer

NDAL Mfg Inc. is recalling ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray because the product was confirmed to have yeast contamination. The recall affects 4,265 bottles distributed nationwide in the USA and Hong Kong. The record does not specify a remedy or action for consumers. Read more at govinfonow.com/recall/36602-manukaguard-nasal-spray-recall-yeast-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/36602-manukaguard-nasal-spray-recall-yeast-contamination-risk · Updated October 11, 2026 · FDA enforcement record: FDA #D-0269-2021

Cite this page

“ManukaGuard Nasal Spray Recall: Yeast Contamination Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/36602-manukaguard-nasal-spray-recall-yeast-contamination-risk. Based on FDA recall #D-0269-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0269-2021%22&limit=1).

The FDA announced on Dec. 17, 2020, that NDAL Mfg Inc. is recalling ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray due to microbial contamination confirmed to have yeast. Owners should stop using the product immediately.

How to tell if you have it

Brand: ManukaGuard
Product: Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270 measured sprays
UPC: 8 58631 00212 8
Lot #: 2010045
Best Before: 10 2023

The hazard

The product is confirmed to have yeast, posing a risk of microbial contamination in non-sterile products. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show other recent recalls of similar products include ClearLife Allergy Nasal Spray Recall (2025-12-12), Medinatura ReBoost Nasal Spray Recall (2025-12-12), and Beekeeper's Naturals Saline Nasal Spray Recall (2026-06-01).

How to tell if you have this one

Look for a 1.3 FL OZ (40mL) bottle with 270 measured sprays. Check the label for UPC 8 58631 00212 8, Lot # 2010045, and Best Before 10 2023.

Brand
ManukaGuard
Product
ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270 measured sprays
Category
Drug

Based on the official FDA remedy

What to do — step by step

Stop using the product
Discontinue use of the recalled ManukaGuard Nasal Spray immediately due to yeast contamination.
Check your lot number
Verify if your bottle has Lot # 2010045 and Best Before 10 2023 to confirm it is part of this recall.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Distributed Nationwide in the USA and Hong Kong” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 2 months after the firm started it.

Dec 17, 2020Firm started the recall
Feb 19, 2021FDA classified it Class I
Mar 3, 2021Published in FDA’s Enforcement Report

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

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Link to this recall

<a href="https://govinfonow.com/recall/36602-manukaguard-nasal-spray-recall-yeast-contamination-risk">ManukaGuard Nasal Spray Recall: Yeast Contamination Risk (GovInfoNow)</a>

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-0269-2021 (December 17, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0269-2021 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.