# FDA recall D-1449-2014

> **Shamrock Medical Solutions Group LLC** · Class II · drug recall initiated 2011-09-27.

## Product

Pramipexole Dihydrochloride Tablets, 0.5 mg, Rx, packaged and labeled to contain Nebivolol tablets, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Northstar Rx, Memphis, TN   NDC 16714-586-01

## Reason for recall

Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets

## Distribution

Product was shipped to the following states: CO, MA, OH, TX & WY.

## Key facts

- **Recall number:** D-1449-2014
- **Recalling firm:** Shamrock Medical Solutions Group LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2011-09-27
- **Report date:** 2014-07-30
- **Termination date:** 2014-07-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lewis Center, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1449-2014

## Citation

> AI Analytics. FDA recall D-1449-2014. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-1449-2014. Source: US FDA. Licensed CC0.

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