OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product… — Class II food recall F-1821-2014
Terminated recall by Magno Humphries Laboratories, Inc, reported 2014-04-23, distributed nationwide. Magno Humphries Laboratories is recalling Vitamin E softgels because the principle display panel states the pr
| Recall number | F-1821-2014 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Magno Humphries Laboratories, Inc, Tigard, OR, United States |
| Recall initiated | 2014-03-25 |
| Classified | 2014-04-11 |
| Reported by FDA | 2014-04-23 |
| Terminated | 2014-11-07 |
| Distributed | Nationwide (US) |
| Quantity | 2,376 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00043292562917 |
Product
OPTIMUM E-1000 IU Gluten Free Dietary Supplement 100 SOFTGELS Product is packaged in a white HDPE bottle with foil cap under the white plastic cap. Bottle contains 100 softgel caps. UPC 0 43292 56291 7.
Reason for recall
Magno Humphries Laboratories is recalling Vitamin E softgels because the principle display panel states the product contains 1000 IU of Vitamin E however the Supplement Facts label indicated 200 IU of Vitamin E. The supplement actually contains 1000 IU of Vitamin E.
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/F-1821-2014. 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.