Abbott recalls ARCHITECT C Peptide Reagents due to a Mexico license renewal error. All units until new license is obtained are affected. No remedy specified in recall notice.
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 Reagents because of a license renewal error in Mexico. This affects all units until a new license is obtained. The recall does not include a specific remedy.
The recall is due to an error in the renewal documentation process for a license in Mexico. This means the reagents may not be legally authorized for use in Mexico until a new license is obtained. The hazard does not involve physical safety risks but legal compliance issues.
Healthcare providers using ARCHITECT C Peptide Reagents for diabetes diagnosis are affected. Patients using these reagents for abnormal insulin secretion testing may be at risk if the reagents are not properly licensed.
Check the lot numbers: 01719F000 (expires May 14, 2020) and 02519E000 (expires April 9, 2020). These reagents are used for diagnosing abnormal insulin secretion in patients with diabetes.
Look for lot numbers 01719F000 (expires May 14, 2020) or 02519E000 (expires April 9, 2020) on the reagent packaging.
The recall is due to an error in the renewal documentation process for a license in Mexico. All reagents are affected until a new license is obtained.
The recall notice does not specify a remedy. Check the lot numbers to see if your reagent is affected.
The recall is related to legal compliance in Mexico, not physical safety risks. No injury risk is described.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1893-2020 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1893-2020 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.
