Walmart Swab
FDA Recall NDC 49035-814

FDA Enforcement Report: View Recall Date, Reasons, and Safety Status

Active & Historical Enforcement Reports

The FDA has identified 1 recorded enforcement report(s) associated with Walmart (NDC 49035-814). A significant event, classified as Class II, was initiated on Jul 07, 2025 by Walmart Inc.. The reported reason for this action was: "Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration."

This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.

Reported Recall Events

July 2025 Class II Recall: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

Recall Number
Class II Ongoing
Reason for Recall
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Initiated
Jul 07, 2025
Reported
Sep 03, 2025
Quantity
3,456,000 pads

Recall Profile & Regulatory Data

Event ID
97385
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
MEDLINE INDUSTRIES, LP - Northfield
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
Nationwide
Product Description
ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per case), NDC 49035-814-60.
Batch or Lot Expiration Information
Lot# 61224070073
Affected Packages Involved in this Recall
49035-814-30Product
49035-814-60Product
6122407007Product

About FDA Recall Enforcement Reports

FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.

If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.