# FDA recall D-007-2013

> **Paddock Laboratories, LLC** · Class II · drug recall initiated 2012-10-03.

## Product

Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,

## Reason for recall

Paddock Laboratories, LLC are recalling one lot   (2012028142) of Moexipril HCl Tablets 7.5mg (expiration 1/2014) because of a  non-conformity dissolution failure result found during routine stability testing at the 6 month test interval.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-007-2013
- **Recalling firm:** Paddock Laboratories, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-10-03
- **Report date:** 2012-10-17
- **Termination date:** 2013-11-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-007-2013

## Citation

> AI Analytics. FDA recall D-007-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-007-2013. Source: US FDA. Licensed CC0.

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