RecallHawk

Woolite Delicates detergent in 50-fluid-ounce bottles

Reckitt Benckiser LLC, of Parsippany, New Jersey

Summary

CPSC recalled 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 or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.. Remedy: Consumers should immediately stop using the recalled Woolite Delicates detergent with lot codes S24364, S24365 and S24366 and contact Reckitt for a full refund. To receive a refund, consumers should write their name and "Recalled" in permanent marker on the back of the product, then take a photo with the UPC and lot code visible, and email the photo to ConsumerCare_USA@reckitt.com. Once consumers receive their refund, they should dispose of the product by closing the bottle tightly and placing it in household trash. Do not empty the product prior to disposal. Do not attempt to recycle the product bottle..

Details

Source

cpsc

External ID

25189

Action Date

2025-03-20

Status

Ongoing

Category

product

Product Description

This recall involves 50-fluid-ounce bottles of Woolite Delicates detergent (SKU 62338-72724) with lot codes S24364, S24365 and S24366, sold exclusively on Amazon.com. The lot code is printed at the top of the back of the bottle. The bottles are white with a light pink label and cap.

Context & Analysis

Reckitt Benckiser LLC, of Parsippany, New Jersey has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for product

Related Actions