Abbott recalls specific Hemoglobin A1c test kits that may produce falsely elevated blood sugar readings. Affected kits include certain lots from 2023. Users should contact Abbott for details.
There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
Abbott is recalling specific Hemoglobin A1c test kits that may give falsely high blood sugar results. This could lead to incorrect diabetes management decisions if used without knowing the issue.
These test kits may produce falsely elevated Hemoglobin A1c results when used with Abbott's Architect or Alinity c systems. This could lead to incorrect diabetes management decisions if users rely on the results.
People using Abbott Hemoglobin A1c test kits for diabetes monitoring may be affected. Those with diabetes who rely on these tests for accurate blood sugar tracking are most at risk.
Check the lot numbers: 59588UQ04, 59868UQ05, 59900UQ06, 60138UQ07, 60237UQ08, 60535UQ08, 60698UQ09, 60880UQ10, 61066UQ01, 61246UQ01, 61250UQ01. The kits are sold with specific model numbers and quantities.
Look for lot numbers 59588UQ04 through 61250UQ01 on the test kit packaging.
The test kits may produce falsely elevated Hemoglobin A1c results when used with Abbott's Architect or Alinity c systems, which could lead to incorrect diabetes management decisions.
Contact Abbott directly to confirm if your kit is affected and get instructions on what to do next.
The recall is for potential false results, not direct health risks. However, incorrect diabetes management could occur if users rely on these results.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1454-2022 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1454-2022 from Abbott. 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.
