Haimen Shengbang recalls HX-K59 Activated Viral Transport Containers 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 all HX-K59 Activated Type Viral Transport Containers sold in the US because they were distributed without proper VTM guidance clearance. This could lead to improper handling of biological samples.
The containers were distributed without following VTM (Viral Transport Medium) guidance and without clearance. This could result in improper handling of biological samples, potentially leading to contamination or safety issues.
Users of the HX-K59 Viral Transport Containers in the US are affected. Laboratory staff handling biological samples are most at risk.
Check for the model number HX-K59 on the container. All units distributed in the US are affected, with no unique device identifiers.
Look for the model number HX-K59 on the container. All US-distributed units are affected.
The containers were distributed without following VTM guidance and without clearance, which could lead to improper handling of biological samples.
The recall record does not specify a return or remedy action.
The recall record does not describe a specific injury risk or hazard mechanism.
We’ve drafted a message you can send Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. to request your refund or repair — edit it as you like.
Subject: Recall Z-1398-2022 — Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. Haimen Sheng: Haimen Shengbang Laborat Hello, I own a Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd. that is covered by recall Z-1398-2022 from Haimen Sheng: Haimen Shengbang Laboratory Equipment Co. Ltd.. 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.
