Abbott recalls ARCHITECT HbA1c Calibrators delivered without dry ice. This may cause calibration errors in diabetes testing. Affected units: Lot 90292050: 100 units.
Devices were delivered without the required dry ice.
Abbott is recalling ARCHITECT HbA1c Calibrators that were shipped without dry ice. This could lead to inaccurate diabetes test results if used without proper calibration.
The calibrators were delivered without dry ice, which is needed to keep them stable during shipping. Without dry ice, the calibrators may become unstable and provide inaccurate test results.
People using these calibrators for diabetes testing may be affected. Those with diabetes who rely on accurate HbA1c measurements are most at risk.
Check for the lot number 902920500 on the packaging. The product was sold as part of the ARCHITECT i System for diabetes testing.
Look for lot number 902920500 on the packaging to confirm if your calibrator is affected.
Dry ice is required to maintain the calibrators' stability during shipping. Without it, the product may become unstable.
100 units with lot number 902920500 were affected.
No, but you should check the lot number to ensure you have an affected unit. If you do, contact Abbott for guidance.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1356-2019 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1356-2019 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.
