Cerovite Liquid — Class II food recall F-0258-2017
Terminated recall by Pharmatech LLC, reported 2016-11-02, distributed in FL, MI, MS, OH. Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia c
| Recall number | F-0258-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmatech LLC, Davie, FL, United States |
| Recall initiated | 2016-08-08 |
| Classified | 2016-10-25 |
| Reported by FDA | 2016-11-02 |
| Terminated | 2024-09-23 |
| Distributed | FL, MI, MS, OH |
| Quantity | 129,268 bottles |
| Pathogens | burkholderia |
| UPC / GTIN / UDI-DI | 00005362790590 |
| Lot numbers | 20471516, 20471517, 20471518, 20471519, 20471520, 20471521, 20471601, 20471608, 20471610, 20471613, 20471614 |
| Expiration dates | 2017-11, 2017-12, 2018-01, 2018-04, 2018-05, 2018-06 |
Product
Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
Reason for recall
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
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-0258-2017. 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.