Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD
Summary
The FDA issued a Class II for Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: by Medical Products Laboratories, Inc.. Reason: Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis.
Details
Source
Drug Recall
External ID
D-0179-2026
Action Date
2025-12-03
Status
Ongoing
Category
drug
Product Description
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/Code Info: Lot#: 71409, Expires: 02/28/2027; 71861, Expires: 08/31/2027.
Quantity Affected: 41,328 bottles
Reason for Recall
Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
Distribution
Nationwide USA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-12
Company
Philadelphia, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 47 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Medical Products Laboratories, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Medical Products Laboratories, Inc. have FDA actions?
This is the only FDA action we have on record for Medical Products Laboratories, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0179-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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