Threshold Enterprises Ltd recalls Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180
Planetary Herbals is recalling Mullein Lung Complex products due to a labeling error indicating incorrect inactive ingredients. Consumers should check product numbers and lot dates for affected items.
Lower-risk recall
Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).
Contact the company & request your remedy
What happened, in plain English
Planetary Herbals is recalling several sizes of Mullein Lung Complex supplements because of a labeling error that shows the wrong inactive ingredients. This error doesn't pose a safety risk but could cause confusion about the product's composition. Read more at govinfonow.com/recall/17996-planetary-herbals-mullein-lung-complex-recall-labeling-error-in-inactive.
Source Summary by GovInfoNow · govinfonow.com/recall/17996-planetary-herbals-mullein-lung-complex-recall-labeling-error-in-inactive · Updated October 5, 2026 · FDA enforcement record: FDA #F-1097-2019
Cite this page
“Planetary Herbals Mullein Lung Complex Recall: Labeling Error in Inactive Ingredients.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17996-planetary-herbals-mullein-lung-complex-recall-labeling-error-in-inactive. Based on FDA recall #F-1097-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1097-2019%22&limit=1).
Why it’s dangerous
The recall is due to a labeling error that incorrectly lists the inactive ingredients in the product. This error does not cause physical harm but could lead to confusion about the product's actual composition.
Who’s affected
Anyone who owns or uses Planetary Herbals Mullein Lung Complex supplements with the listed item numbers and lot dates. People who rely on the product for respiratory health may be most affected by the labeling error.
How to tell if you have this one
Check for product numbers PF0003 (15 count), PF0002 (90 count), PF0106 (180 count), or PF7013 (90+90 count). Look for lot numbers and expiry dates listed in the description.
- Brand
Planetary Herbals- Category
Food
What to do — step by step
Check Product Details
Review the product number and lot date on the bottle to confirm if it matches the recalled items listed in the notice.
Questions people ask
Is this product safe to use?
Yes, the product is safe but the labeling error means the inactive ingredients listed may not match what's actually in the product.
What should I do if I have the product?
The official notice does not specify a remedy, so you can continue using it but should check the product details to confirm if it's affected.
How can I tell if my product is recalled?
Check for product numbers PF0003, PF0002, PF0106, or PF7013 with the specific lot dates listed in the recall notice.
Contact Planetary Herbals
We’ve drafted a message you can send Planetary Herbals to request your refund or repair — edit it as you like.
Subject: Recall F-1097-2019 — Planetary Herbals Planetary Herbals Hello, I own a Planetary Herbals that is covered by recall F-1097-2019 from Planetary Herbals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1097-2019 (December 7, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1097-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.