Abbott recalls ARCHITECT C Peptide Calibrators due to Mexico license renewal documentation error. All units until new license is obtained are affected. No immediate action needed but check lot numbers.
Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.
Abbott is recalling ARCHITECT C Peptide Calibrators because of a Mexico license renewal documentation error. This affects all units until a new license is obtained. The recall does not require immediate action but users should check their lot numbers.
The recall is due to an error in Mexico's license renewal documentation process. This means the product may not be legally authorized for use until a new license is obtained. The hazard is a regulatory compliance issue, not a direct safety risk.
Healthcare facilities using ARCHITECT C Peptide Calibrators for diabetes testing are affected. Patients using these calibrators for abnormal insulin secretion diagnosis are at risk if the license issue continues.
Check the lot number on the calibrator, which is listed as 01819G000. The expiration date is June 12, 2020. This product is used for diabetes testing and abnormal insulin secretion diagnosis.
Look for the lot number 01819G000 on the calibrator packaging.
Abbott recalls ARCHITECT C Peptide Calibrators due to an error in Mexico's license renewal documentation process.
The recall is a regulatory compliance issue, not a direct safety risk. No injuries are reported.
Check the lot number on the calibrator; the recalled lot is 01819G000 with an expiration date of June 12, 2020.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1895-2020 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1895-2020 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.
