Celltrion recalls specific lots of DiaTrust COVID-19 Ag Rapid Test kits due to incorrect expiration dates. Consumers should check their lot numbers to determine if affected.
Kits were labeled with incorrect expiration dates.
Celltrion is recalling certain lots of its DiaTrust COVID-19 Ag Rapid Test kits because they have incorrect expiration dates. This could lead to inaccurate test results if used after the wrong expiration date.
The kits have incorrect expiration dates, which means they might expire before the actual expiration date. Using them after the wrong expiration date could lead to inaccurate test results.
Anyone who purchased the specific lot numbers listed (COVGCCM0006 to COVGCCM1007) of the Celltrion DiaTrust COVID-19 Ag Rapid Test kits. People using these kits for testing are most at risk of inaccurate results.
Check the lot number on the test kit packaging. Affected lots are COVGCCM0006, COVGCCM0007, COVGCCM0008, COVGCCM1002, COVGCCM1003, COVGCCM1004, COVGCCM1005, COVGCCM1006, and COVGCCM1007.
Look for the lot number on the test kit packaging to see if it matches the affected lots listed: COVGCCM0006 to COVGCCM1007.
The recall is happening because the kits have incorrect expiration dates, which could lead to inaccurate test results if used after the wrong expiration date.
Check the lot number on the test kit packaging. If it matches the affected lots (COVGCCM0006 to COVGCCM1007), you should stop using it and contact Celltrion for further instructions.
The recall specifically lists the affected lot numbers. Check the lot number on the packaging to see if it matches COVGCCM0006 through COVGCCM1007.
We’ve drafted a message you can send Celltrion to request your refund or repair — edit it as you like.
Subject: Recall Z-0731-2022 — Celltrion Celltrion Hello, I own a Celltrion that is covered by recall Z-0731-2022 from Celltrion. 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.
