Xenesta Nuvive Womens 90 count packaged in a white plastic bottle… — Class I food recall F-0915-2018
Terminated recall by Progressive Laboratories, Inc, reported 2018-03-21, distributed nationwide. Recalled dietary supplements may contain undeclared milk.
| Recall number | F-0915-2018 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Progressive Laboratories, Inc, Irving, TX, United States |
| Recall initiated | 2018-02-23 |
| Classified | 2018-03-13 |
| Reported by FDA | 2018-03-21 |
| Terminated | 2018-08-07 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen |
| Allergens | milk |
| Lot numbers | 2071957, 2082387 |
Product
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Reason for recall
Recalled dietary supplements may contain undeclared milk.
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-0915-2018. 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.