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Stop using now Drug recall · FDA · Published December 12, 2025

ClearLife Allergy Nasal Spray Recall: Microbial Contamination Risk

Medinatura recalls ClearLife Allergy Nasal Spray, Extra Strength due to yeast/mold and Achromobacter contamination. Check your bottle.

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

🇺🇸 FDA recall #D-0289-2026DrugClearLife ›
Official FDA recall photos · click to enlarge
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Contact the company

Recalling firmMedinatura New Mexico, inc.10421 Research Rd Se · Albuquerque, NM 87123-3423
✎ GovInfoNow plain-language explainer

Medinatura New Mexico, Inc. is recalling ClearLife Allergy Nasal Spray, Extra Strength (0.68 fl. oz.) because the non-sterile product contains microbial contamination identified as yeast, mold, and Achromobacter. This recall covers all lots within their expiry dates distributed nationwide in the US. The record does not currently list a specific remedy or return process for consumers. Read more at govinfonow.com/recall/31617-clearlife-allergy-nasal-spray-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/31617-clearlife-allergy-nasal-spray-recall-microbial-contamination-risk · Updated October 9, 2026 · FDA enforcement record: FDA #D-0289-2026

Cite this page

“ClearLife Allergy Nasal Spray Recall: Microbial Contamination Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/31617-clearlife-allergy-nasal-spray-recall-microbial-contamination-risk. Based on FDA recall #D-0289-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0289-2026%22&limit=1).

The FDA announced on Dec. 12, 2025, that Medinatura New Mexico, Inc. is voluntarily recalling ClearLife Allergy Nasal Spray, Extra Strength due to microbial contamination. The agency said the non-sterile products contain yeast/mold and Achromobacter.

How to tell if you have it

  • ClearLife Allergy Nasal Spray, Extra Strength
  • 0.68 fl. oz. (20 mL) bottles
  • UPC 787647101887
  • NDC 62795-4006-9
  • Distributed by MediNatura

The hazard

According to the FDA, the products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. The recall is classified as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Beekeeper's Naturals Saline Nasal Spray Recall (2026-06-01) and Walgreens Saline Nasal Spray with Xylitol Recall (2025-11-12). Clear Eyes Eye Drops Recalled for Sterility Risk was reported on 2026-07-29.

How to tell if you have this one

Check your bottle for the brand name 'ClearLife' and the description 'Allergy Nasal Spray, Extra Strength'. Verify the size is 0.68 fl. oz. (20 mL) bottles distributed by MediNatura. Look for NDC 62795-4006-9 and UPC 787647101887 on the packaging.

  • Brand
    ClearLife
  • Product
    ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Ongoing
  • Distribution
    Nationwide in the US
Recall numberProduct, codes & lotsQuantityNDC
D-0288-2026ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863; All lots within expiry.—62795-4005-9, 7876471018
D-0289-2026ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887; All lots within expiry.—62795-4006-9, 7876471018
Based on the official FDA remedy

What to do — step by step

  1. Stop Using the Product

    Discontinue use of the recalled ClearLife Allergy Nasal Spray immediately due to microbial contamination risks.

  2. Check Your Bottle Details

    Verify if your bottle matches NDC 62795-4006-9 and UPC 787647101887.

  3. Monitor for Official Updates

    Since the remedy is not currently stated in the record, watch for updates from Medinatura regarding returns or refunds.

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 in the US” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 33 days after the firm started it.

1. Firm started the recall: Dec 12, 202512. Published in FDA’s Enforcement Report: Jan 14, 202623. FDA classified it Class I: Jan 15, 2026320252026
  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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Keep exploring

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-0289-2026 (December 12, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0289-2026 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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