RecallHawk
Class II Recall

BARRIER THERAPY SKIN PROTECTANT CREAM (1% colloidal oatmeal), 10 FL OZ/296 ML- tube, Distributed By: Prequel, LOS ANGELE

PREQUEL SKIN

Summary

The FDA issued a Class II for BARRIER THERAPY SKIN PROTECTANT CREAM (1% colloidal oatmeal), 10 FL OZ/296 ML- t by PREQUEL SKIN. Reason: Microbial contamination of non-sterile Products -.

Details

Source

Drug Recall

External ID

D-0657-2024

Action Date

2024-09-18

Status

Ongoing

Category

drug

Product Description

BARRIER THERAPY SKIN PROTECTANT CREAM (1% colloidal oatmeal), 10 FL OZ/296 ML- tube, Distributed By: Prequel, LOS ANGELES, CA 90069. UPC 8 10129 11007 4

Lot/Code Info: Lot: X4054A, Exp: 2/2026; X4136A, X4137A, X4138A, Exp: 5/2026

Quantity Affected: 30,946 tubes

Reason for Recall

Microbial contamination of non-sterile Products -

Distribution

Distributed nationwide in USA and on line

Type: Voluntary: Firm initiated

Recall Initiated: 2024-08-28

Company

PREQUEL SKIN

W Hollywood, CA

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 24 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 (PREQUEL SKIN) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does PREQUEL SKIN have FDA actions?

This is the only FDA action we have on record for PREQUEL SKIN in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0657-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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