FDAClass IIMay 16, 2018

Metoprolol Succinate Extended-Release Tablets recall

Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited…

Why was Metoprolol Succinate Extended-Release Tablets recalled?

Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Batch # C706254, 08/2019

Product
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited…
Recalling firm
Dr. Reddy's Laboratories, Inc.
Quantity
8160 bottles
Distribution
Nationwide
Recall date
May 16, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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