Super Colon Cleanse — Class III drug recall D-1406-2012
Terminated recall by Health Plus Incorporated, reported 2012-07-11, distributed nationwide. Labeling: Label Mix-up: The product is being recalled because active ingredient in the Drug Facts box incorrec
| Recall number | D-1406-2012 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Health Plus Incorporated, Chino, CA, United States |
| Recall initiated | 2012-06-28 |
| Classified | 2012-07-03 |
| Reported by FDA | 2012-07-11 |
| Terminated | 2013-01-15 |
| Distributed | Nationwide (US) |
| Quantity | 24,423 bottles |
| Reason classes | labeling |
| Lot numbers | 120201286, 120502276 |
| Expiration dates | 2015-03, 2015-05 |
Product
Super Colon Cleanse, stimulant laxative, 140 mg of Senna per capsule, 25 doses, 100 capsules, Manufactured by: healthPLUS Inc. Chino, CA 91710 USA.
Reason for recall
Labeling: Label Mix-up: The product is being recalled because active ingredient in the Drug Facts box incorrectly states "Active Ingredients per dose" Senna Leaf powder 140 mg. It should correctly be stated as "Active ingredient (in each capsule)" Senna Leaf Powder 140 mg.It should correctly be stated as Active ingredient (in each capsule) Senna Leaf Powder 140 mg.
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-1406-2012. 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.