Radiometer recalls AQURE REF 933-599 software versions 2.5.2 through 2.6.1 due to potential patient information mix-ups. Affected medical devices may require software updates to prevent errors in patient data management.
Due to potential software issue that may result in patient mix-up information.
Radiometer is recalling specific software versions of its AQURE system for medical use. The issue could lead to patient information mix-ups, which might cause errors in medical testing and reporting.
The software issue could cause patient data to be mixed up during testing, potentially leading to incorrect medical results. This might happen if the system fails to properly link patient information with test results.
Healthcare professionals using the AQURE system for patient data management are most at risk. The recall affects medical devices sold to hospitals and clinics that use these software versions.
Check if your AQURE system has model number 933-599 and software versions 2.5.2 through 2.6.1. The system is used in medical settings for managing patient data and test results.
Identify your AQURE system's software version by checking the device settings or documentation.
Contact Radiometer to get the latest software update to fix the patient data mix-up issue.
Software versions 2.5.2, 2.5.3, 2.5.4, 2.6.0, and 2.6.1 are affected.
Check if your AQURE system has model number 933-599 and software versions 2.5.2 through 2.6.1.
The recall states there is a potential for patient information mix-ups, but no specific risk of serious injury is mentioned.
We’ve drafted a message you can send Radiometer to request your refund or repair — edit it as you like.
Subject: Recall Z-1394-2023 — Radiometer Radiometer Hello, I own a Radiometer that is covered by recall Z-1394-2023 from Radiometer. 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.
