Krishe recalls disposable sampling tubes (REF VSM01) due to lack of FDA verification before sale. All lots affected. No remedy specified in official recall.
Verification and validation of the virus transport medium tubes was not provided to FDA prior to sale and marketing
Krishe is recalling disposable sampling tubes (REF VSM01) because they were sold without proper FDA verification. This means the tubes may not meet safety standards for virus transport.
The tubes were sold without FDA verification, meaning they might not meet safety standards for handling viruses. This could lead to improper testing results or contamination risks if not properly validated.
Users of these sampling tubes for medical testing are affected. Healthcare providers and labs using the tubes are most at risk.
Check for the REF VSM01 label on the tube packaging. The product includes 50 transport media tubes, 50 nasal swabs, and a package insert. All lots are affected.
Look for the REF VSM01 label on the tube packaging to confirm it's affected.
The tubes were sold without proper FDA verification before marketing, which means they may not meet safety standards for virus transport.
The official recall does not specify any remedy.
Check the product label for REF VSM01. If you have the affected tubes, you should contact Krishe for guidance.
We’ve drafted a message you can send Krishe to request your refund or repair — edit it as you like.
Subject: Recall Z-1420-2021 — Krishe Krishe Hello, I own a Krishe that is covered by recall Z-1420-2021 from Krishe. 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.