PSYLLIUM FIBER — Class III drug recall D-1315-2014
Terminated recall by Konsyl Pharmaceuticals Inc, reported 2014-05-21, distributed in FL, MN, NY, OH, OR, PA, PR, SC…. Labeling: Label Error on Declared Strength; Listed active ingredient strength is inaccurate.
| Recall number | D-1315-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Konsyl Pharmaceuticals Inc, Easton, MD, United States |
| Recall initiated | 2014-04-01 |
| Classified | 2014-05-13 |
| Reported by FDA | 2014-05-21 |
| Terminated | 2016-05-26 |
| Distributed | FL, MN, NY, OH, OR, PA, PR, SC, TX |
| Countries outside the US | DO |
| Quantity | 6,286 bottles |
| Reason classes | labeling, potency |
| NDC | 00224-1847-10 |
| Lot numbers | A44701 |
Product
PSYLLIUM FIBER, Laxative/Supplement, 100 Capsules, OTC. Manufactured By: Konsyl Pharmaceuticals, Inc., Easton, MD 21601. NDC: 0224-1847-10.
Reason for recall
Labeling: Label Error on Declared Strength; Listed active ingredient strength is inaccurate.
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-1315-2014. 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.