Recalls / Class I
Class ID-0945-2019
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 #5 Fire Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4205-2
- Affected lot / code info
- Lots: NR-022318E Exp. 02/20; NR-030418A Exp. 03/20; NR-051618D Exp. 05/20; NR-051818D Exp. 05/20; NR-081017E Exp. 08/19; NR-120317E Exp. 12/19; NR-121517A Exp. 12/19; NR-031516J Exp. 3/19; NR-010617E Exp. 01/20; NR011216H Exp. 01/19; NR-040417C Exp. 4/20; NR-050916D Exp. 5/19; NR-061517A Exp. 6/20; NR-061616D Exp. 6/19; NR-080116A Exp. 8/19; NR090115J Exp. 9/18; NR-090916B Exp. 9/19; NR-101416E Exp. 10/19; NR-120815K Exp.12/18
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
- 19490 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-0945-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.