Haimen Shengbang recalls Genesis Biomedical Viral Transport Container Model HX-K59-1 due to distributed VTM outside VTM Guidance without clearance. All US-distributed units affected.
Distributed VTM outside of VTM Guidance and without clearance.
Haimen Shengbang is recalling their Genesis Biomedical Viral Transport Container (Model HX-K59-1) because it was distributed without proper clearance for VTM (Viral Transport Medium) guidelines. This could lead to improper handling of samples and potential contamination risks.
The container was distributed without clearance for VTM (Viral Transport Medium) guidelines. This means it may not be properly designed or certified for handling infectious samples, increasing the risk of sample contamination or improper transport.
Users of the Genesis Biomedical Viral Transport Container Model HX-K59-1 in the US are affected. Laboratory personnel handling infectious samples are most at risk.
Check for the model number HX-K59-1 on the container. All units distributed in the US are affected, and there is no unique device identifier (UDI).
Look for the model number HX-K59-1 on the container. All US-distributed units are affected.
The recall record states the container was distributed without clearance for VTM guidelines, so it is not safe for proper use with infectious samples.
Check for the model number HX-K59-1 on the container. All units distributed in the US are affected, and there is no unique device identifier (UDI).
The recall record does not specify a remedy, so the official notice does not provide instructions on what to do next.
We’ve drafted a message you can send Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. is the manufacturer. The brand display should be short and human-friendly. to request your refund or repair — edit it as you like.
Subject: Recall Z-1399-2022 — Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. is the manufacturer. The brand display Hello, I own a Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. is the manufacturer. The brand display should be short and human-friendly. that is covered by recall Z-1399-2022 from Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. is the manufacturer. The brand display should be short and human-friendly.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
