Life Technologies recalls StemPro MSC SFM CTS devices with specific lot numbers due to untested supplier components. Affected units may have adventitious agents that could pose health risks.
Component was not tested by the supplier for adventitious agents
Life Technologies is recalling StemPro MSC SFM CTS devices with certain lot numbers because components were not tested by the supplier for potential contaminants. This could lead to health risks if the devices are used without proper testing.
The hazard involves components that were not tested by the supplier for adventitious agents, which are unintended substances that could cause health issues. This lack of testing means the devices might contain contaminants that could pose risks during use.
Users of StemPro MSC SFM CTS devices with the listed lot numbers are affected. Individuals using these devices for laboratory or medical purposes may be at higher risk due to potential contamination.
Check the lot number on your StemPro MSC SFM CTS device. The affected lot numbers include 556094 (expiring 2/28/2010), 577934 (expiring 4/30/2010), and others listed in the recall notice.
Identify the lot number on your StemPro MSC SFM CTS device to see if it matches the affected numbers listed in the recall.
The product was recalled because components were not tested by the supplier for adventitious agents, which could pose health risks.
Affected lot numbers include 556094 (expiring 2/28/2010), 577934 (expiring 4/30/2010), 883643 (expiring 12/30/2011), and others listed in the recall notice.
The recall does not specify a stop-use action, so you do not need to stop using it immediately unless you have an affected lot number.
We’ve drafted a message you can send Life Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0274-2020 — Life Technologies Life Technologies Hello, I own a Life Technologies that is covered by recall Z-0274-2020 from Life Technologies. 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.
