Haimen Shengbang Laboratory Equipment Co. Ltd.

FDA Regulatory Profile

Haimen Shengbang Laboratory Equipment Co. Ltd. appears in FDA public data with 3 recalls — including 3 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1398-2022, Class I) was initiated on July 12, 2022.

Summary

Total Recalls
3 (3 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1398-2022Class IHXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated TypeJuly 12, 2022
Z-1399-2022Class IHXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1July 12, 2022
Z-1400-2022Class IHXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom MadeJuly 12, 2022