The Recall Desk

Manufacturer

Haimen Shengbang Laboratory Equipment Co. Ltd.

3 recalls in our database name Haimen Shengbang Laboratory Equipment Co. Ltd. as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
3
Most recent
2022-08-17

Of the 3 recalls from Haimen Shengbang Laboratory Equipment Co. Ltd. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (100%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–3 of 3

  • SevereFDA (Devices)·Z-1398-2022·2022-08-17

    FDA Recalls Viral Transport Containers Distributed Without Clearance

    FDA recalls approximately 8.7 million viral transport containers that were distributed without regulatory clearance and without complying with FDA guidance for proper viral transport specifications.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1400-2022·2022-08-17

    Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance

    Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1399-2022·2022-08-17

    FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance

    The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
    Category
    Medical Device
    Distribution
    Distributed nationwide