FDA Drug Recalls

Recalls / Class I

Class ID-0637-2019

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

Dr. King's Natural Medicine Homeopathic Snore Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512028, NDC 57955-5120-2

Affected lot / code info
Lots: 052516Y Exp. 05/19; 060518C Exp. 06/20; 060917F Exp. 06/19; 070518A Exp. 07/20; 080317C Exp. 08/19; 081015B Exp. 08/18; 081815G Exp. 08/18; 111516C Exp. 11/19; 112317E 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
14781 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-0637-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class I recall: drug · FDA Drug Recalls