Pramipexole Dihydrochloride Tablets — Class II drug recall D-1449-2014
Terminated recall by Shamrock Medical Solutions Group LLC, reported 2014-07-30, distributed in CO, MA, OH, TX, WY. Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochl
| Recall number | D-1449-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Shamrock Medical Solutions Group LLC, Lewis Center, OH, United States |
| Recall initiated | 2011-09-27 |
| Classified | 2014-07-23 |
| Reported by FDA | 2014-07-30 |
| Terminated | 2014-07-31 |
| Distributed | CO, MA, OH, TX, WY |
| Quantity | 99 |
| Reason classes | labeling |
| NDC | 16714-0586-01 |
| Lot numbers | 002B90 |
| Expiration dates | 2012-12-14 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1449-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.