FDA recall F-3356-2017

Product

Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels

Reason for recall

Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.

Distribution

Domestic distribution only.

Key facts

Status

Terminated

Initiation date

2017-07-21

Report date

2017-08-16

Termination date

2019-04-24

Voluntary/Mandated

Voluntary: Firm initiated

Location

Doral, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-3356-2017