FDA Drug recall D-1128-2017
Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By: Watson Pharmaceut…
- FDA Drug
- Class III
- terminated
- Published 2017-09-13
On 2017-09-13 the FDA classified a Class III recall of Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By: Watson Pharmaceut… by Mckesson Packaging Services, citing failed moisture limits: Out of specification for moisture content.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1128-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-08-28 |
| Published | 2017-09-13 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Mckesson Packaging Services |
| Distribution | CO, IL, LA, OH, PA |
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
Failed moisture limits: Out of specification for moisture content.
Identifiers
| code_info | Lot#: 0112313 Exp. 12/2017; 0113376 Exp. 06/2018; 0113645 Exp. 02/2019. |
|---|
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-1128-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.