Recall Number: F-3356-2017
Why was Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels recalled?
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Check out this page for guidance on what to do if you've consumed food from recall F-3356-2017 .
City: Doral
State: Florida
Country: United States
Classification: Class II
Classification Date: 2017-08-08
Reason: Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Product Description: Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Report Date: 2017-08-16
Product Type: Food
Company: Duy Drugs Inc.
Status: Terminated
Recall Number: F-3356-2017
Postal Code: 33126-1111
Recall Initiation Date: 2017-07-21
Recall End Date: 2019-04-24
Event ID: 77715
Distribution Pattern: Domestic distribution only.
Voluntary Or Mandated: Voluntary: Firm initiated
Initial Firm Notification: E-Mail
Extra Info: Lot No. 1701
Product Quantity: 411 bottles
Address: 1730 NW 79th Ave
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