Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 7, 2018 (8 years ago)

Planetary Herbals Mullein Lung Complex recall

Recalled by Threshold Enterprises Ltd · Scotts Valley, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Recall of Mullein Lung Complex due to a labeling error which indicates the incorrect excipient profile (inactive ingredients).

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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

Quantity: 16, 542 units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

15 count lot number and expiry dates: FG-85657 - 1/21 FG-90863 - 11/21 FG-94415 - 4/22 FG-96010 - 7/22 90 count: FG-84056 - 1/21 FG-90862 - 11/21 FG-94413 - 4/22 FG-96008 - 7/22 180 count: FG-84057 - 1/21 FG-87851 - 1/21 FG-90864 - 11/21 FG-94414 - 4/22 FG-96009 - 7/22 90 + 90 Count: FG-90865 - 11/21 FG-96011 - 7/22

Where it was sold

Nationwide.

FDA's distribution note: Nationwide distribution

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Threshold Enterprises Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 7, 2018
In FDA report of
Mar 6, 2019
Terminated
Jun 7, 2019
FDA recall number
F-1097-2019 · event 82088
Official record
FDA enforcement report search

Other recalls by Threshold Enterprises Ltd

Class II · Moderate risk Terminated Other

Planetary Herbals Ginseng Classic

Reason Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.

Threshold Enterprises Ltd 7 states F-3338-2017
Class II · Moderate risk Terminated Labeling

Source Naturals Dietary Supplement Vitamin D-3

Reason Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.

Threshold Enterprises Ltd Nationwide F-2178-2017