# FDA recall D-1447-2014

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

## Product

Oxycodone HCl Oral Concentrate, 20 mg/mL, Rx (C-II) Packaged and labeled as Morphine Sulfate 20 mg/mL, Mfg: Lannett Co. Inc., Re-Packaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfr: Cody Laboratories Inc., Cody, WY  NDC 00527-1426-36

## Reason for recall

Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL

## Distribution

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

## Key facts

- **Recall number:** D-1447-2014
- **Recalling firm:** Shamrock Medical Solutions Group LLC
- **Classification:** Class I
- **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-1447-2014

## Citation

> AI Analytics. FDA recall D-1447-2014. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1447-2014. Source: US FDA. Licensed CC0.

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