Morphine Sulfate Immediate Release tablet — Class I drug recall D-1386-2012
Terminated recall by Physicians Total Care, Inc, reported 2012-06-27, distributed in FL. Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may contain Morphine Sulfate ER and vic
| Recall number | D-1386-2012 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physicians Total Care, Inc, Tulsa, OK, United States |
| Recall initiated | 2010-11-10 |
| Classified | 2012-06-18 |
| Reported by FDA | 2012-06-27 |
| Terminated | 2012-07-24 |
| Distributed | FL |
| Reason classes | labeling |
| NDC | 54868-4973-00 |
| Lot numbers | 65J2 |
| Expiration dates | 2012-06-30 |
Product
Morphine Sulfate Immediate Release tablet, 30 mg/120 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, OK 74146-6234, NDC 54868-4973-00
Reason for recall
Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may contain Morphine Sulfate ER and vice-versa.
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-1386-2012. 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.