Planetary Herbals Mullein Lung Complex — Class II food recall F-1097-2019
Terminated recall by Threshold Enterprises Ltd, reported 2019-03-06, distributed nationwide. Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inacti
| Recall number | F-1097-2019 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Threshold Enterprises Ltd, Scotts Valley, CA, United States |
| Recall initiated | 2018-12-07 |
| Classified | 2019-02-26 |
| Reported by FDA | 2019-03-06 |
| Terminated | 2019-06-07 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | 1/21, 11/21, 4/22, 7/22, FG-85657, FG-90863, FG-94415, FG-96010 |
| Model numbers | PF0002, PF0003, PF0106 |
Product
Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180 count, Item number PF0106 and 90 + 90 count, PF 7013 white plastic bottles. Proprietary Blend: Platycodon root, Ophiopagon Rhizome, Long Pepper Fruit, Black Cherry Bark, Cassia Bark, Elecampane Root, Mullein Leaf, Licorice Root and Ginger Rhizome Extract. Manufactured for: Planetary Herbals LLC. P.O. Box 1760, Soquel, CA 95073
Reason for recall
Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1097-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.