FDA Food recall F-3356-2017
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
- FDA Food
- Class II
- terminated
- Published 2017-08-16
On 2017-08-16 the FDA classified a Class II recall of Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels by Duy Drugs, citing failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-3356-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-21 |
| Published | 2017-08-16 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Duy Drugs |
| Distribution | n/a |
Product
Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels
Reason
Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.
Identifiers
| code_info | Lot No. 1701 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3356-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.