FDA Food recall F-0258-2017
Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile
- FDA Food
- Class II
- terminated
- Published 2016-11-02
On 2016-11-02 the FDA classified a Class II recall of Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile by Pharmatech, citing recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0258-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-08 |
| Published | 2016-11-02 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Pharmatech |
| Distribution | FL, MI, MS, OH |
Product
Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
Reason
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Identifiers
| upc | 005362790590 |
|---|---|
| code_info | UPC No. 005362790590; Lot No. 20471516, 20471517, 20471518, 20471519, & 20471520, Exp. Date 11/2017; Lot No. 20471521,…UPC No. 005362790590; Lot No. 20471516, 20471517, 20471518, 20471519, & 20471520, Exp. Date 11/2017; Lot No. 20471521, Exp. Date 12/2017; Lot No. 20471601, Exp. Date 01/2018; Lot No. 20471608, Exp. Date 04/2018; Lot No. 20471610 & 20471613, Exp. Date 05/2018; Lot No. 20471614, Exp. Date 06/2018. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0258-2017%22
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