CLASS I Food recall · Reported 21 Mar 2018 · FDA Enforcement Report
Xenesta Nuvive Womens recalled by Progressive Laboratories
Progressive Laboratories is recalling Xenesta Nuvive Womens, distributed nationwide in the US. The recall was initiated on 23 Feb 2018 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0915-2018
- FDA event ID
- 79350
- Recalling firm
- Progressive Laboratories, Irving, TX
- Brand
- Xenesta Nuvive
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 23 Feb 2018
- FDA classified
- 13 Mar 2018
- Reported
- 21 Mar 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Milk
- Product category
- Other
Timeline
| 23 Feb 2018 | Recall initiated by company | |
| 13 Mar 2018 | Classified by FDA | +18 days |
| 21 Mar 2018 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Recalled dietary supplements may contain undeclared milk.
Product as listed by the FDA
Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap
Where it was distributed
Nationwide through the United States
Questions about this recall
Is Xenesta Nuvive Womens recalled?
Yes. Progressive Laboratories recalled Xenesta Nuvive Womens on 23 Feb 2018. The recall is Class I and its status is Terminated. Recall number F-0915-2018.
Why was it recalled?
Recalled dietary supplements may contain undeclared milk.
Which lots are affected?
Lot # 2071957 and 2082387
Where was it sold?
Nationwide through the United States
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Progressive Laboratories
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Xenesta Nuvive Mens recalled by Progressive LaboratoriesXenesta Nuvive | Progressive Laboratories | Undeclared Milk | Nationwide |
| Food | CLASS I | Testosterzone 180 count bottle packaged in an amber plastic bottle recalledTestosterzone | Progressive Laboratories | Undeclared Milk | Nationwide |
| Food | CLASS I | Thyroid Resilience recalled by Progressive LaboratoriesThyroid Resilience | Progressive Laboratories | Undeclared Milk | Nationwide |
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