HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1 — FDA record Z-1399-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 12, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
Reason
Distributed VTM outside of VTM Guidance and without clearance.
Classification
Class I
Recalling firm
Haimen Shengbang Laboratory Equipment Co. Ltd.
Quantity
3,950,000 total units
Agency-reported status
Ongoing
Source record identifier
Z-1399-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityNo UDI. All lots distributed in the US.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide distribution - US Nationwide distribution in the states of CA, FL, IL & NY. The country of China.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Aug 17, 2022
Recall initiation date
Jul 12, 2022
Center classification date
Aug 8, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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