Breckenridge Pharmaceutical, Inc.
3
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Drug
2026-05-13 to 2026-06-17
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-06-17 | FDA Drug | FDA Recall: Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Tow | Breckenridge Pharmaceutical, Inc. | Class II | N/A |
| 2026-06-17 | FDA Drug | FDA Recall: Duloxetine Delayed-Release Capsules, USP, 60mg, packaged in a) 90 Capsules (NDC 51991-748-90); b) 10 | Breckenridge Pharmaceutical, Inc. | Class II | N/A |
| 2026-05-13 | FDA Drug | FDA Recall: Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutica | Breckenridge Pharmaceutical, Inc. | Class II | N/A |