CLASS II Drug recall · Reported 13 Feb 2019 · FDA Enforcement Report

Medline Remedy Essential Barrier Skin Protectant Ointment recalled

US Pharmaceuticals is recalling Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%), distributed nationwide in the US. The recall was initiated on 7 Dec 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # a) and b): 44G17, Exp. 05/2019
Quantity recalled7020 units

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-0427-2019
FDA event ID
81784
Recalling firm
US Pharmaceuticals, Belleville, NJ
Classification
Class II
Status
Terminated
Recall initiated
7 Dec 2018
FDA classified
4 Feb 2019
Reported
13 Feb 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

7 Dec 2018Recall initiated by company
4 Feb 2019Classified by FDA+59 days
13 Feb 2019Published in enforcement report+9 days

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

Reason for recall

GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample

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

Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%) packaged in a) 2 oz tubes (NDC 53329-302-14) and b) 6 oz tubes (NDC 53329-302-41), Medline Industries Inc., Manufactured for Medline Industries Inc., Mundelien, IL 60060.

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Why was it recalled?

GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample

Which lots are affected?

Lot # a) and b): 44G17, Exp. 05/2019

Where was it sold?

Nationwide within the United States

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

2 other products · FDA event 81784

This product is part of a recall event; the main page for the event is Soothe & Cool Protect Moisture Guard Skin Protectant recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IISoothe & Cool Protect Moisture Guard Skin Protectant recalledUS PharmaceuticalsPotency & AssayNationwide
CLASS IIHydrocortisone Cream 1% MS Anti itch Cream recalledHydrocortisone Cream Intensive HealingUS PharmaceuticalsPotency & AssayNationwide

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