D-0952-2019 Class I Terminated

Recalled by King Bio Inc. — Asheville, NC

FDA drug recall D-0952-2019 was initiated by King Bio Inc. on Jul 20, 2018 and is designated Class I. Reason for recall: Microbial contamination The recall status is terminated (terminated Jan 19, 2022). Affected quantity: 14695 bottles.

Recall Details

Product Type
Drugs
Report Date
Mar 20, 2019
Initiation Date
Jul 20, 2018
Termination Date
Jan 19, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
14695 bottles

Product Description

NET Remedies #11 Visceral Polarity Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4211-2

Reason for Recall

Microbial contamination

Distribution Pattern

U.S.A. Nationwide, Canada, and Australia.

Code Information

Lots: NR-031516D Exp. 03/19; NR-073015H Exp. 07/18; NR-010617K Exp. 01/20; NR-011216A Exp. 01/19; NR-050916B Exp. 05/19; NR-061616J Exp. 06/19; NR-080116J Exp. 08/19; NR-090115D Exp. 09/18; NR-090816A Exp. 09/19; NR-101416J Exp. 10/19; NR-120815F Exp. 12/18; NR-020118M Exp. 02/20; NR-072617A Exp. 07/19; NR-110117C Exp. 11/19; NR-120317L Exp. 12/19

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0952-2019
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 12, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.