# FDA recall D-0606-2017

> **Legacy Pharmaceutical Packaging LLC** · Class II · drug recall initiated 2017-03-07.

## Product

ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH  45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ  08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.

## Reason for recall

Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.

## Distribution

Product was shipped to distribution centers in TN, IN, and AZ then further shipped the product to retail pharmacies nationwide in the USA.

## Key facts

- **Recall number:** D-0606-2017
- **Recalling firm:** Legacy Pharmaceutical Packaging LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-03-07
- **Report date:** 2017-03-29
- **Termination date:** 2019-08-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Earth City, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0606-2017

## Citation

> AI Analytics. FDA recall D-0606-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0606-2017. Source: US FDA. Licensed CC0.

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