Abbott Laboratories is a global leader in medical devices, diagnostics, and healthcare products. We provide innovative solutions for healthcare professionals and patients worldwide.
Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues found in the Alinity ci-series System software versions 3.6.1. and lower that could lead to erroneous results for multiple analytes. The issue was identified by Abbott during the internal testing of complaint investigations.
Abbott Laboratories is a leading global company in the medical device, diagnostics, and healthcare products industry. They offer innovative solutions for healthcare professionals and patients across the world.
The company is a legitimate and well-established healthcare provider with no known risks associated with their products. They are a major player in the medical device and diagnostics industry.
Healthcare professionals and patients
Check for official Abbott Laboratories product labels and packaging for safety information.
Verify the product's official label or packaging for the manufacturer's name and product details.
Ensure the product is registered with the appropriate regulatory bodies (e.g., FDA in the United States).
Consult the product's user manual or online resources for safety instructions and warnings.
Yes, Abbott Laboratories is a well-established global company with a long history in the medical device and diagnostics industry.
Abbott products undergo rigorous testing and quality control to ensure safety and efficacy. Always follow the instructions provided with the product.
Contact Abbott's customer support or visit their official website to report any safety concerns.
We’ve drafted a message you can send Abbott Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-0961-2026 — Abbott Laboratories Abbott Laboratories Hello, I own a Abbott Laboratories that is covered by recall Z-0961-2026 from Abbott Laboratories. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
