F-0275-2017 Class II Terminated

Recalled by Pharmatech LLC — Davie, FL

FDA food recall F-0275-2017 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: 62,228 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
62,228 bottles

Product Description

Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 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

Lot No. 30161601, Exp. Date 01/2018; Lot No. 30161602 & 30161603.

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0275-2017
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 23, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.