FDA Drug recall D-1447-2014
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 B…
- FDA Drug
- Class I
- terminated
- Published 2014-07-30
On 2014-07-30 the FDA classified a Class I recall of 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 B… by Shamrock Medical Solutions Group, citing labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1447-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2011-09-27 |
| Published | 2014-07-30 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Shamrock Medical Solutions Group |
| Distribution | CO, MA, OH, TX, WY |
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
Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL actually contained OxyCODONE HCl 20 mg/mL
Identifiers
| code_info | Lot #: 002HZI Use By: 7/20/2013 NDC: 00527-1426-36 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1447-2014%22
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