Recall
FDAHealthNovember 22, 2025

Changchun Wancheng Bio-Electron Co., Ltd. — LH One Step Ovulation Test Device (Urine)

⚠️ Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
November 22, 2025

US Nationwide distribution in the states of TX, GA, CA.

What's affected?

Product
LH One Step Ovulation Test Device (Urine)
Lot code
(Expiration):

Additional details

Name/Lot(Expiration): LH One Step Ovulation Test Device (Urine)/GT-LH 20251601(05-2027)

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 1,000.

View original FDA notice →

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