RecallHawk

Woolite Delicates detergent in 50-fluid-ounce bottles

Reckitt Benckiser LLC, of Parsippany, New Jersey

Summary

CPSC recall: Woolite Delicates detergent in 50-fluid-ounce bottles. By Reckitt Benckiser LLC, of Parsippany, New Jersey. Hazard: The recalled products can contain Pseudomonas species bacteria, including Pseudomonas oleovorans, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to the bacteria face a risk of serious infection that may require medical treatment. The bacteria can enter the body through the eyes o

Details

Source

CPSC Consumer Product Recall

External ID

10207

Action Date

2025-03-20

Status

Recalled

Category

consumer_product

Product Description

This recall involves 50-fluid-ounce bottles of Woolite Delicates detergent (SKU 62338-72724) with lot codes S24364, S243

Context & Analysis

This is a unclassified recall.

This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Reckitt Benckiser LLC, of Parsippany, New Jersey 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 (Reckitt Benckiser LLC, of Parsippany, New Jersey) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Reckitt Benckiser LLC, of Parsippany, New Jersey have FDA actions?

Reckitt Benckiser LLC, of Parsippany, New Jersey 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 "10207" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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