# FDA recall D-0754-2021

> **RemedyRepack Inc.** · Class II · drug recall initiated 2021-08-17.

## Product

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

## Reason for recall

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

## Distribution

Product was distributed to two medical facilities in VA and FL.

## Key facts

- **Recall number:** D-0754-2021
- **Recalling firm:** RemedyRepack Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-08-17
- **Report date:** 2021-09-01
- **Termination date:** 2022-03-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indiana, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0754-2021

## Citation

> AI Analytics. FDA recall D-0754-2021. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/D-0754-2021. Source: US FDA. Licensed CC0.

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