D-0949-2019 Class I Terminated
FDA drug recall D-0949-2019 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: 14249 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
- 14249 bottles
Product Description
NET Remedies #20 Pain Relief Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4213-2
Reason for Recall
Microbial contamination
Distribution Pattern
U.S.A. Nationwide, Canada, and Australia.
Code Information
Lots: NR-010617M Exp. 01/20; NR-031516C Exp. 03/19; NR-061616L Exp. 06/19; NR-090115F Exp. 09/18; NR-090616M Exp. 09/19; NR-101416L Exp. 10/19; NR-120815C Exp. 12/18; NR-020118P Exp. 02/20; NR-022318K Exp. 02/20; NR-022318M Exp. 02/20; NR-052517A Exp. 05/20; NR-060517F Exp. 06/20; NR-060618A Exp. 06/20; NR-061418A Exp. 06/20; NR-121417B 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-0949-2019
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026