Haimen Shengbang recalls custom-made viral transport containers distributed without VTM clearance. No UDI. All US lots affected.
Distributed VTM outside of VTM Guidance and without clearance.
Haimen Shengbang's custom viral transport containers were distributed without proper VTM clearance. This could lead to improper handling of biological samples.
Distributed VTM (Viral Transport Medium) outside of VTM guidance without clearance means improper handling of biological samples. This could lead to contamination or safety risks.
Lab users and healthcare professionals who handle biological samples with these containers are most at risk. All US-distributed lots are affected.
Look for Haimen Shengbang custom-made viral transport containers with no UDI. All US-distributed lots are affected.
Look for the absence of a UDI (Unique Device Identifier) on the container.
The containers were distributed without proper VTM clearance, which could lead to improper handling of biological samples.
The recall record does not specify a remedy, so check with the manufacturer for guidance.
The recall indicates potential improper handling risks, but the exact hazard is not clearly described.
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. to request your refund or repair — edit it as you like.
Subject: Recall Z-1400-2022 — 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. that is covered by recall Z-1400-2022 from Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. is the manufacturer. The brand display should be short and human.. 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.
