# FDA recall D-1036-2016

> **Sandoz Inc** · Class III · drug recall initiated 2016-05-25.

## Product

Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only,  Manufactured by Sandoz  Inc., Princeton, NJ 08540, NDC 0185-0630-01

## Reason for recall

Labeling: Incorrect or Missing Package Insert

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1036-2016
- **Recalling firm:** Sandoz Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-05-25
- **Report date:** 2016-06-22
- **Termination date:** 2017-04-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1036-2016

## Citation

> AI Analytics. FDA recall D-1036-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1036-2016. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*