Wise Woman Herbals Sleepytime Glycerite — Class II food recall F-1348-2022

Terminated recall by EarthLab Inc, reported 2022-06-29, distributed nationwide. The microbial test result is found to be out of specification due to high yeast and mold counts.

Recall number	`F-1348-2022`
Product type	Food
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	EarthLab Inc, Creswell, OR, United States
Recall initiated	2022-05-11
Classified	2022-06-22
Reported by FDA	2022-06-29
Terminated	2023-05-22
Distributed	Nationwide (US)
Reason classes	microbial contamination, specification failure
Pathogens	mold, yeast
UPC / GTIN / UDI-DI	`00748840142695`, `00748840142701`, `00748840142718`, `00748840142725`, `00748840142732`
Lot numbers	`16905`, `16963`, `17019`, `17338`, `17648`, `17724`, `17950`

Product

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

Reason for recall

The microbial test result is found to be out of specification due to high yeast and mold counts.

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-1348-2022. 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.