FDA Drug Recalls

Recalls / Class I

Class ID-0943-2019

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

NET Remedies #1 Earth Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4201-2

Affected lot / code info
Lots: NR-031516N Exp. 03/19; NR-073015C Exp. 07/18; NR-010617A Exp. 01/20; NR-011216L Exp. 01/19; NR-021717A Exp. 02/20; NR-050916E Exp. 05/19; NR-060517A Exp. 06/20; NR-061616A Exp. 06/19; NR-080116D Exp. 08/19; NR-090115C Exp. 09/18; NR-090616A Exp. 09/19; NR-101416A Exp. 10/19; NR-120815A Exp. 12/18; NR-020118A Exp. 02/20; NR-022318A Exp. 02/20; NR-051618B Exp. 05/20; NR-071718E Exp. 07/20; NR-110817A Exp. 11/19; NR-103117A Exp. 10/19; NR-120317A Exp. 12/19

Why it was recalled

Microbial contamination

Recalling firm

Firm
King Bio Inc.
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
3 Westside Dr, N/A, Asheville, North Carolina 28806-2846

Distribution

Quantity
17395 bottles
Distribution pattern
U.S.A. Nationwide, Canada, and Australia.

Timeline

Recall initiated
2018-07-20
FDA classified
2019-03-08
Posted by FDA
2019-03-20
Terminated
2022-01-19
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0943-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.