Recalls / Class I
Class ID-0950-2019
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 #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2
- Affected lot / code info
- Lots: NR-031516H Exp. 03/19; NR-011216G Exp. 01/19; NR-021717C Exp. 02/20; NR-040417D Exp. 04/20; NR-061616E Exp. 06/19; NR-090115H Exp. 09/19; NR-090616E Exp. 09/19; NR-101416F Exp. 10/19; NR-120815L Exp. 12/18; NR-020118F Exp. 02/20; NR-022318F Exp. 02/20; NR-052218A Exp. 05/20; NR-071718G Exp. 07/20; NR-101117G Exp. 10/19; NR-120317F Exp. 02/19; NR-110117D Exp. 11/19
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
- 11489 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-0950-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.