RecallHawk

Imatinib Mesylate Tablets 100 mg, Imatinib Mesylate Tablets 400 mg, Pregabalin Capsules 50 mg, Pregabalin Capsules 75 mg

Dr. Reddy's Laboratories, Ltd., of India

Summary

CPSC recall: Imatinib Mesylate Tablets 100 mg, Imatinib Mesylate Tablets 400 mg, Pregabalin Capsules 50 mg, Pregabalin Capsules 75 mg, Pregabalin Capsules 100 mg, Pregabalin Capsules 150 mg, Sevelamer Carbonate Tablets 800 mg, Tadalafil Tablets 5 mg and Tadalafil Tablets 20 mg. By Dr. Reddy's Laboratories, Ltd., of India. Hazard: The products are prescription medications that were labeled and distributed by Dr. Reddy's for institutional use only. The prescription medications were distributed by

Details

Source

CPSC Consumer Product Recall

External ID

9007

Action Date

2021-02-25

Status

Recalled

Category

consumer_product

Product Description

This recall involves blister packages of prescription medications. The name and strength of the medication, "For Institu

Context & Analysis

This is a unclassified recall.

This was one of 7 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Dr. Reddy's Laboratories, Ltd., of India 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 (Dr. Reddy's Laboratories, Ltd., of India) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Dr. Reddy's Laboratories, Ltd., of India have FDA actions?

Dr. Reddy's Laboratories, Ltd., of India 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 "9007" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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