FDAClass IISeptember 1, 2021

Carvedilol 25 mg recall

Carvedilol 25 mg, 180-count bottle, Rx only, Manufactured by Zydus Pharm, Pennington, NJ 08534, NDC 68382-0095-05, Repackaged by RemedyRepack Inc.…

Why was Carvedilol 25 mg recalled?

A 500 count bottle of Carvedilol 25 mg tablets contained two Paroxetine Tablets, 40 mg. Product was repackaged into 180 count bottles.

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?

Lot # B1273286-071521, Exp 07/31/2022

Product
Carvedilol 25 mg, 180-count bottle, Rx only, Manufactured by Zydus Pharm, Pennington, NJ 08534, NDC 68382-0095-05, Repackaged by RemedyRepack Inc.…
Recalling firm
RemedyRepack Inc.
Quantity
4
Distribution
Product was distributed to two medical facilities in VA and FL.
Recall date
September 1, 2021
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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