# FDA recall D-1026-2020

> **Perrigo Company PLC** · Class II · drug recall initiated 2019-10-23.

## Product

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-01; NDC Berkley Jensen: 68391-852-56; NDC: CVS Health: 59779-540-01; NDC DG Health: 55910-011-01; NDC Kirkland: 63981-852-56; NDC Kroger: 30142-600-56; NDC Meijer: 41250-852-01; NDC Rite Aid: 11822-0852-4; NDC Walgreens: 0363-0852-01

## Reason for recall

CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

## Distribution

Nationwide USA

## Key facts

- **Recall number:** D-1026-2020
- **Recalling firm:** Perrigo Company PLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-10-23
- **Report date:** 2020-03-25
- **Termination date:** 2020-11-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allegan, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1026-2020

## Citation

> AI Analytics. FDA recall D-1026-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1026-2020. Source: US FDA. Licensed CC0.

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