FDA Food recall F-1448-2020
Mitmitta (Cayenne Pepper)
- FDA Food
- Class II
- terminated
- Published 2020-09-09
On 2020-09-09 the FDA classified a Class II recall of Mitmitta (Cayenne Pepper) by Sundial Herbal Products, citing recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1448-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-30 |
| Published | 2020-09-09 |
| Last updated | 2026-09-13 11:50 UTC |
| Company | Sundial Herbal Products |
| Distribution | NY |
Product
Mitmitta (Cayenne Pepper); "Traditional Uses: Prevents heart attacks, and lowers high blood pressure, stops internal bleeding, Heals ulcers and pains there of: Improves circulation, thins blood and keeps it moving***"
Reason
Recall required by Order of Permanent Injunction. The products are misbranded and deemed unapproved drugs based on labeling claims.
Identifiers
| code_info | Product manufactured, processed, packed, held, and/or distributed during the time period beginning 1/1/2014 through 5/27/2020. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1448-2020%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.