BRANMOOR
THURSDAY · 14 MAY 2026

FDA Recall D-0949-2019

King Bio Inc. · Asheville, NC

Class I — life-threatening Terminated 1279 days on record

Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death.

Product

NET Remedies #20 Pain Relief Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4213-2

Lot / code: 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

Quantity: 14249 bottles

Reason for recall

Microbial contamination

Recall record

Recall number
D-0949-2019
Classification
Class I
Status
Terminated
Voluntary or mandated
Voluntary: Firm initiated
Firm notification
Press Release
Distribution
U.S.A. Nationwide, Canada, and Australia.
Recall initiated
2018-07-20
Classified by FDA Center
2019-03-08
FDA published
2019-03-20
Terminated
2022-01-19
Recalling firm
King Bio Inc.
Firm location
Asheville, NC

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