Vectornate recalls MedSchen: Smart Transport Medium System due to discoloration and turbidity in some lots from South Korean facility during Monsoon season.
Discoloration and turbidity were present in the specified lots of STMs because of Longer Monsoon season at the South Korean Manufacturing Facility.
Vectornate is recalling certain MedSchenker Smart Transport Medium (STM) systems because they may have discoloration and turbidity due to manufacturing conditions in South Korea. This could affect the reliability of clinical specimen transport.
Discoloration and turbidity in the STM system may occur due to the South Korean manufacturing facility's Monsoon season conditions. This could potentially affect the system's ability to properly transport clinical specimens.
Healthcare workers using the MedSchenker STM system for clinical specimen transport are most at risk. The recall applies to specific serial and lot numbers.
Check for serial number STM-UNV-0001-Q121 and lot number JAH161 on the product. The product is used for clinical specimen transport from collection sites to testing labs.
Look for serial number STM-UNV-0001-Q121 and lot number JAH161 on the MedSchenker STM system.
The MedSchenker Smart Transport Medium system may have discoloration and turbidity due to manufacturing conditions at the South Korean facility during Monsoon season.
Check for serial number STM-UNV-0001-Q121 and lot number JAH161. If you have these numbers, contact Vectornate for guidance.
The recall record does not specify a remedy.
We’ve drafted a message you can send Vectornate to request your refund or repair — edit it as you like.
Subject: Recall Z-1417-2021 — Vectornate Vectornate Hello, I own a Vectornate that is covered by recall Z-1417-2021 from Vectornate. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.