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Unrated Drug recall · FDA · Published November 12, 2025

Walgreens Saline Nasal Spray with Xylitol Recall: Microbial Contamination Risk

Walgreens Saline Nasal Spray with Xylitol (1.5 oz) recalled due to pseudomonas lactis contamination. Stop using affected lots before expiration.

🇺🇸 FDA recall #D-0179-2026DrugMedical Products Laboratories ›
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Recalling firmMedical Products Laboratories, Inc.9990 Global Rd · Philadelphia, PA 19115-1006
✎ GovInfoNow plain-language explainer

Walgreens Saline Nasal Spray with Xylitol (1.5 oz) bottles are recalled because they were contaminated with pseudomonas lactis. This contamination could cause infection if used improperly. Read more at govinfonow.com/recall/31640-walgreens-saline-nasal-spray-with-xylitol-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/31640-walgreens-saline-nasal-spray-with-xylitol-recall-microbial-contamination-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0179-2026

Cite this page

“Walgreens Saline Nasal Spray with Xylitol Recall: Microbial Contamination Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/31640-walgreens-saline-nasal-spray-with-xylitol-recall-microbial-contamination-risk. Based on FDA recall #D-0179-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0179-2026%22&limit=1).

The FDA announced on Nov. 12, 2025, that Medical Products Laboratories, Inc. is recalling Walgreens Saline Nasal Spray WITH XYLITOL due to microbial contamination risk. The firm initiated the voluntary Class II recall after pseudomonas lactis was found in the product.

How to tell if you have it

  • Brand: Medical Products Laboratories
  • Product: Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle
  • Distributed by: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015
  • NDC: 0363-3114-01
  • Lot codes: 71409 (Expires: 02/28/2027), 71861 (Expires: 08/31/2027)
  • Units affected: 41,328 bottles

The hazard

The product is contaminated with the microorganism pseudomonas lactis. The FDA classified this as a Class II recall because ingestion or use could cause serious health problems.

Context

GovInfoNow's records show other recent recalls of similar products include Beekeeper's Naturals Saline Nasal Spray Recall (2026-06-01), 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 the 1.5 oz (45mL) bottle with lot numbers 71409 (expires 02/28/2027) or 71861 (expires 08/31/2027).

  • Brand
    Medical Products Laboratories
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot numbers 71409 or 71861 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 USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 21 days after the firm started it.

1. Firm started the recall: Nov 12, 202512. FDA classified it Class II: Nov 21, 202523. Published in FDA’s Enforcement Report: Dec 3, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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-0179-2026 (November 12, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0179-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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