FDA Drug recall D-1119-2017
Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories,…
- FDA Drug
- Class II
- terminated
- Published 2017-08-30
On 2017-08-30 the FDA classified a Class II recall of Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories,… by The Harvard Drug Group, citing microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1119-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-02 |
| Published | 2017-08-30 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | The Harvard Drug Group |
| Distribution | US |
Product
Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85
Reason
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Identifiers
| code_info | Item# 370010, Lot: 20351701 |
|---|
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-1119-2017%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.