Abbott recalls ARCHITECT Intact PTH Calibrators due to delivery without required dry ice. This may affect calibration accuracy for PTH testing in blood samples.
Devices were delivered without the required dry ice.
Abbott is recalling ARCHITECT Intact P: PTH Calibrators because they were delivered without the required dry ice. This could lead to inaccurate PTH testing results in blood samples.
The calibrators were delivered without dry ice, which is necessary for proper storage. Without dry ice, the calibrators may not function correctly, leading to inaccurate PTH test results.
Healthcare facilities using these calibrators for PTH testing in blood samples. Patients receiving PTH tests may be affected if their results are inaccurate.
Check for the model number LN 8K25-12 and lot number 01018I000 on the calibrators. These items were sold by Abbott Laboratories.
Look for model number LN 8K25-12 and lot number 01018I000 on the calibrators.
The calibrators were delivered without the required dry ice, which is necessary for proper storage and accurate testing.
Inaccurate PTH test results could occur if the calibrators are used without dry ice.
Check for model number LN 8K25-12 and lot number 01018I000 on the calibrators.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1357-2019 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1357-2019 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.
