CLASS II ONGOING Drug recall · Reported 3 Sep 2025 · FDA Enforcement Report

ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs recalled

Medline Industries LP - Northfield is recalling ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, distributed nationwide in the US. The recall was initiated on 7 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes61224070073
NDC49035-814
Quantity recalled3,456,000 pads

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0602-2025
FDA event ID
97385
Recalling firm
Medline Industries LP - Northfield, Northfield, IL
Brand
Walmart
Manufacturer
Walmart Inc.
Classification
Class II
Status
Ongoing
Recall initiated
7 Jul 2025
FDA classified
26 Aug 2025
Reported
3 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

7 Jul 2025Recall initiated by company
26 Aug 2025Classified by FDA+50 days
3 Sep 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

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.

Where it was distributed

Nationwide

Nationwide

Stores named: Walmart

Questions about this recall

Why was it recalled?

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

Which lots are affected?

61224070073

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

5 other products · FDA event 97385

This product is part of a recall event; the main page for the event is Good Neighbor Pharmacy, Alcohol Prep Pads recalled.

More recalls from Medline Industries LP - Northfield

All 792

Other Isopropyl Alcohol recalls

All 11