Life Technologies recalls Oncomine Dx Target Test RNA/DNA Panel for NSCLC detection due to extended expiration date prior to clearance. Affected lots may expire before intended use.
Extended Expiration Date prior to clearance
Life Technologies is recalling its Oncomine Dx Target Test RNA/DNA Panel for non-small cell lung cancer detection because the expiration date may extend beyond the clearance period. This could lead to expired tests being used after their intended validity.
The test panels have an extended expiration date that may expire before the intended clearance period. This could result in expired tests being used after their expiration date, potentially affecting test accuracy.
Healthcare providers using the Oncomine Dx Target Test RNA/DNA Panel for non-small cell lung cancer detection are likely affected. Patients receiving tests from these providers may be at risk if expired tests are used.
Check for Catalog Number A32441 and Lot Codes S119_2174743, S119_2188760, S119_2165333, P119_2149298, S217_04001, 1705002. The product was sold with a unique device identifier (UDI) starting with (01)10190302015103.
Verify the expiration date against the intended clearance period to ensure it hasn't expired.
The recall is due to an extended expiration date that may expire before the intended clearance period, potentially affecting test accuracy.
Affected lots include S119_2174743, S119_2188760, S119_2165333, P119_2149298, S217_04001, and 1705002.
Look for Catalog Number A32441 and the listed Lot Codes on the product label.
We’ve drafted a message you can send Life Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1706-2020 — Life Technologies Life Technologies Hello, I own a Life Technologies that is covered by recall Z-1706-2020 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.
