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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90602

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 12, 2022
Product types
Device
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
Haimen Shengbang Laboratory Equipment Co. Ltd.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type

Z-1398-2022
Recall number
Z-1398-2022
Initiated
July 12, 2022
Classification
Class I
Status
Ongoing
Quantity
8,710,600total units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Distributed VTM outside of VTM Guidance and without clearance.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Distributed VTM outside of VTM Guidance and without clearance.

Code information

No UDI. All lots distributed in the US.

Distribution pattern

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

device · product 2 of 3

HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1

Z-1399-2022
Recall number
Z-1399-2022
Initiated
July 12, 2022
Classification
Class I
Status
Ongoing
Quantity
3,950,000 total units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Distributed VTM outside of VTM Guidance and without clearance.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Distributed VTM outside of VTM Guidance and without clearance.

Code information

No UDI. All lots distributed in the US.

Distribution pattern

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

device · product 3 of 3

HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made

Z-1400-2022
Recall number
Z-1400-2022
Initiated
July 12, 2022
Classification
Class I
Status
Ongoing
Quantity
100,000 total units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Distributed VTM outside of VTM Guidance and without clearance.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Distributed VTM outside of VTM Guidance and without clearance.

Code information

No UDI. All lots distributed in the US.

Distribution pattern

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