Nature's Only Choice B17 BITTER RAW APRICOT EXTRACT AMYGDALIN Dietary… — Class II food recall F-1480-2018
Terminated recall by Nature's Only Choice, reported 2018-05-30, distributed nationwide. The Vitamin B17 containing product is considered to be a prescription drug, new drug, and unapproved new drug.
| Recall number | F-1480-2018 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nature's Only Choice, Dolgeville, NY, United States |
| Recall initiated | 2018-05-16 |
| Classified | 2018-05-22 |
| Reported by FDA | 2018-05-30 |
| Terminated | 2018-06-29 |
| Distributed | Nationwide (US) |
| Quantity | 250 bottles |
| Reason classes | unapproved product |
| Expiration dates | 2019-06 |
Product
Nature's Only Choice B17 BITTER RAW APRICOT EXTRACT AMYGDALIN Dietary Supplement 100 Capsules
Reason for recall
The Vitamin B17 containing product is considered to be a prescription drug, new drug, and unapproved new drug.
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-1480-2018. 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.