RecallHawk

CVS Health Medicated Hemorrhoidal Wipes

Diamond Wipes International, Inc. of Chino, California

Summary

CPSC recall: CVS Health Medicated Hemorrhoidal Wipes. By Diamond Wipes International, Inc. of Chino, California. Hazard: The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.. Remedy: Consumers should secure the wipes out of sight and reach o

Details

Source

CPSC Consumer Product Recall

External ID

10843

Action Date

2026-07-02

Status

Recalled

Category

consumer_product

Product Description

This recall involves CVS Health Medicated Hemorrhoidal Wipes. The pain-relieving wipes were sold in boxes of 20 individu

Context & Analysis

This is a unclassified recall.

This was one of 22 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Diamond Wipes International, Inc. of Chino, California has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Diamond Wipes International, Inc. of Chino, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Diamond Wipes International, Inc. of Chino, California have FDA actions?

Diamond Wipes International, Inc. of Chino, California has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10843" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for consumer_product

Related Actions