RecallHawk

Walgreens Pain Reliever Acetaminophen, 150 count bottles

Aurobindo Pharma Limited, of Telangana, India

Summary

CPSC recall: Walgreens Pain Reliever Acetaminophen, 150 count bottles. By Aurobindo Pharma Limited, of Telangana, India. Hazard: The recalled over-the-counter products contain the regulated substance acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.. Remedy: Consumers should immediately store the recall

Details

Source

CPSC Consumer Product Recall

External ID

9327

Action Date

2022-06-16

Status

Recalled

Category

consumer_product

Product Description

This recall involves the Walgreens brand acetaminophen product. The red and white label states Walgreens, Easy Open for

Context & Analysis

This is a unclassified recall.

This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Aurobindo Pharma Limited, of Telangana, India has 4 FDA actions in our database, including 2 recalls.

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 (Aurobindo Pharma Limited, of Telangana, India) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Aurobindo Pharma Limited, of Telangana, India have FDA actions?

Aurobindo Pharma Limited, of Telangana, India has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9327" 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