Tosoh Bioscience recalls all lots of ST AIA-PACK FT3 (FT3: Free Triiodothyronine) for in vitro diagnostic use. This product is designed for quantitative measurement of Free Triiodothyronine in human serum or plasma on specific analyzers.
See the official notice for the full hazard description.
Tosoh Bioscience is recalling all lots of ST AIA-PACK FT3 (Free Triiodothyronine) test kits. These are used for in vitro diagnostic purposes on specific analyzers. The recall does not mention a specific hazard or remedy, so no action is needed.
The recall does not specify any hazard or risk. The product is designed for in vitro diagnostic use only, but no safety concerns or issues were identified in the recall notice.
Users of the ST AIA-PACK FT3 test kits for in vitro diagnostic purposes on specific Tosoh AIA System analyzers. Most at risk are healthcare professionals using these kits for laboratory testing.
The product is labeled ST AIA-PACK FT3 (FT3: Free Triiodothyronine) and is used for in vitro diagnostic testing on specific Tosoh AIA System analyzers. All lots are affected.
Look for the product name ST AIA-PACK FT3 (FT3: Free Triiodothyronine) on the label.
The recall does not mention any hazard or risk.
The recall does not specify a remedy, so no action is needed.
The product is labeled ST AIA-PACK FT3 (FT3: Free Triiodothyronine) and is used for in vitro diagnostic testing on specific Tosoh AIA System analyzers. All lots are affected.
We’ve drafted a message you can send Tosoh Biosc: Inc to request your refund or repair — edit it as you like.
Subject: Recall Z-0673-2019 — Tosoh Biosc: Inc Tosoh Biosc: Inc Hello, I own a Tosoh Biosc: Inc that is covered by recall Z-0673-2019 from Tosoh Biosc: Inc. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
