F-0258-2017 Class II Terminated
FDA food recall F-0258-2017 was initiated by Pharmatech LLC on Aug 8, 2016 and is designated Class II. Reason for recall: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia. The recall status is terminated (terminated Sep 23, 2024). Affected quantity: 129,268 bottles.
Recall Details
- Product Type
- Food
- Report Date
- Nov 2, 2016
- Initiation Date
- Aug 8, 2016
- Termination Date
- Sep 23, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 129,268 bottles
Product Description
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.
Distribution Pattern
FL, MI, MS, and OH.
Code Information
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.
Source
- Dataset
- openFDA food recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for F-0258-2017
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 23, 2026