FDAFDA · Food and drugs·Recall number D-0754-2021
Carvedilol 25 mg, 180-count bottle, Rx only, Manufactured by Zydus Pharm, Pennington, NJ 08534, NDC 68382-0095-05, Repackaged by RemedyRepack Inc., Indiana, PA 15701, NDC 70518-1826-01
Published September 1, 2021 · Recall initiated: August 17, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
A 500 count bottle of Carvedilol 25 mg tablets contained two Paroxetine Tablets, 40 mg. Product was repackaged into 180 count bottles.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- RemedyRepack Inc.
- Distributor
- Product was distributed to two medical facilities in VA and FL.
- Lot
- Lot # B1273286-071521, Exp 07/31/2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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