FDA recall F-1458-2018

Product

Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in pouches.

Reason for recall

Samples collected by public health officials found the presence of Salmonella.

Distribution

Recalled product was distributed to retail stores in AZ, IA, ID, IL, KS, MI, UT, and WY.

Key facts

Status

Terminated

Initiation date

2018-03-20

Report date

2018-05-16

Termination date

2019-09-06

Voluntary/Mandated

Voluntary: Firm initiated

Location

Salt Lake City, UT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1458-2018