Recall Z-1400-2022— Haimen Shengbang Laboratory Equipment Co. Ltd.
Class I · Ongoing
Class I FDA medical device recall by Haimen Shengbang Laboratory Equipment Co. Ltd., initiated 2022-07-12. FDA's recall record names no specific 510(k) clearance for this event. Product: HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made. Reason: Distributed VTM outside of VTM Guidance and without clearance..
- Recalling firm
- Haimen Shengbang Laboratory Equipment Co. Ltd.
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2022-07-12
- Firm location
- Nantong, China
Product description
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
Reason for recall
Distributed VTM outside of VTM Guidance and without clearance.
Data sourced from openFDA. This site is unofficial and independent of the FDA.