Thermo Fisher Scientific recalls Samco Bio-Tite Sterile Specimen Containers (120mL) that were not properly irradiated, making them non-sterile and potentially unsafe for lab use. Affected containers have specific catalog numbers and expiration dates.
Product was not irradiated; therefore, they are not sterile and do not meet product specification.
Thermo Fisher Scientific recalls Samco Bio-Tite Sterile Specimen Containers that were not irradiated and therefore not sterile. Using these containers for lab testing could lead to contamination or infection risks.
The containers were not irradiated, so they do not meet sterility specifications. This means they may not be sterile when used for lab testing, potentially leading to contamination or infection risks.
Laboratory users who purchased the Samco Bio-Tite Sterile Specimen Containers with catalog number 07 0006. Those handling specimens for testing are most at risk if the containers are used without proper sterility.
Look for Samco Bio-Tite Sterile Specimen Containers with catalog number 07 0006. The containers have a 120mL size and Bio-Tite Blue Cap. They were manufactured with lot number 1270428 and expire November 19, 2021.
Verify the catalog number, size, and expiration date on the container to confirm if it is affected.
The containers were not irradiated, so they do not meet sterility specifications and are not sterile.
Check the catalog number and expiration date. If affected, contact Thermo Fisher Scientific for guidance.
No, they are not sterile and could lead to contamination or infection risks if used for lab testing.
We’ve drafted a message you can send Thermo Fisher Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2126-2020 — Thermo Fisher Scientific Thermo Fisher Scientific Hello, I own a Thermo Fisher Scientific that is covered by recall Z-2126-2020 from Thermo Fisher Scientific. 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.
