Recalls / Class I
Class ID-0948-2019
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 #2 Metal Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4202-2
- Affected lot / code info
- Lots: NR-031516M Exp. 03/19; NR-073015D Exp. 09/19; NR-010617B Exp. 01/20; NR-011216M Exp. 01/19; NR-042717D Exp. 09/19; NR-051116B Exp. 05/19; NR-061616N Exp. 06/19; NR-080116E Exp. 08/19; NR-090115B Exp. 09/18; NR-090616B Exp. 09/19; NR-101416B Exp. 10/19; NR-120815R Exp. 12/18; NR-081017B Exp. 08/19; NR-020118B Exp. 02/20; NR-022318B Exp. 02/20; NR-101017B Exp. 10/19; NR-120317B 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
- 16495 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-0948-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.