Wise Woman Herbals Kava Capsules
Reason The microbial test result is found to be out of specification due to high yeast and mold counts.
Wise Woman Herbals Sleepytime Glycerite recall
Recalled by EarthLab Inc · Creswell, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The microbial test result is found to be out of specification due to high yeast and mold counts.
Some molds produce toxins, and mold growth usually points to a problem with moisture, packaging or storage. All mold recalls.
What was recalled
Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Boston Round bottle, Black serrated polypropylene dropper assembly with rubber bulb (2oz only) or Black serrated phenolic lid with polypropylene cone insert(4oz and larger), Clear neck band, Wise Woman Herbals label. Each size has the following UPCs: 2 oz UPC 7 48840 14269 5 4 oz UPC 7 48840 14270 1 8 oz UPC 7 48840 14271 8 16 oz UPC 7 48840 14272 5 32 oz UPC 7 48840 14273 2
Quantity: 1 fl oz = 1,010 units; 2 fl oz = 1,219 units; 4 fl oz = 282 units; 8 fl oz = 46 units; 16 fl oz = 16 units; 32 fl oz = 4 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.
2SLGL, 4SLGL, 8SLGL, 16SLGL, 32SLGL. (1st digit indicates package size; SL indicates Sleepytime; GL indicates Glycerite). Lots: 17950, 17724, 17648, 17338, 17019, 16963, 16905. Best if Use for each lot: 10/19/23 (for lot 17950); 3/24/23 (for lot 17724); 3/2/23 (for lot 17648); 9/29/22 (for lot 17338); 11/25/21 (for lot 17019); 9/20/21 (for lot 16963); 8/14/21 (for lot 16905).
Where it was sold
Nationwide.
FDA's distribution note: nationwide
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
- EarthLab Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 11, 2022
- In FDA report of
- Jun 29, 2022
- Terminated
- May 22, 2023
- FDA recall number
- F-1348-2022 · event 90203
- Official record
- FDA enforcement report search
Also recalled with it (2 more products)
FDA files each product of one recall action separately; these share the same FDA event.
Wise Woman Herbals Standardized Kava Glycerite
Reason The microbial test result is found to be out of specification due to high yeast and mold counts.