Propafenone Hydrochloride tablets — Class III drug recall D-1128-2017
Terminated recall by Mckesson Packaging Services, reported 2017-09-13, distributed in CO, IL, LA, OH, PA. Failed moisture limits: Out of specification for moisture content.
| Recall number | D-1128-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Packaging Services, Concord, NC, United States |
| Recall initiated | 2017-08-28 |
| Classified | 2017-09-06 |
| Reported by FDA | 2017-09-13 |
| Terminated | 2020-05-19 |
| Distributed | CO, IL, LA, OH, PA |
| Quantity | 3,966 units |
| Reason classes | specification failure |
| NDC | 63739-0509-10 |
| Lot numbers | 0112313, 0113376, 0113645 |
| Expiration dates | 2017-12, 2018-06, 2019-02 |
Product
Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By: Watson Pharmaceuticals 311 Bonnie Circle Corona, CA 92880, NDC 63739-509-10
Reason for recall
Failed moisture limits: Out of specification for moisture content.
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-1128-2017. 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.