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Recall

Class II — Changchun Wancheng Bio-Electron Co., Ltd.

Recalling firmChangchun Wancheng Bio-Electron Co., Ltd.
Registered facilityCHANGCHUN WANCHENG BIO-ELECTRON CO., LTD. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonTest 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.
ProductVivoo Sodium Test; Vivoo Vitamin C Test; Vivoo Hydration Test
Quantity3,300
DistributionUS Nationwide distribution in the states of TX, GA, CA.
Initiated2025-11-22
Classified2026-02-04
Recall numberZ-1267-2026
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Changchun Wancheng Bio-Electron Co., Ltd. (Z-1267-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97801/

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