Radiometer recalls ABL90 FLEX Analyzers with specific software versions due to security vulnerabilities that may cause shutdowns or reboots, risking delayed medical treatment.
Software Security; The action is being initiated because of software security vulnerabilities with the firm's analyzer operating system, which may cause the device to shutdown or reboot resulting in delayed medical treatment.
Radiometer is recalling ABL90 FLEX Analyzers with certain software versions because security flaws could cause the device to shut down or reboot, potentially delaying critical medical treatments.
The software security vulnerabilities may cause the device to shut down or reboot unexpectedly. This could interrupt medical testing processes and lead to delayed treatment for patients.
Healthcare providers using the ABL90 FLEX Analyzer for medical testing are affected. Those with the specific software versions listed in the recall are most at risk.
Check for the model number ABL90 FLEX Analyzer with reference number REF 393090 and unique device identifier UDI:05700693930909. The affected units have specific software versions: RXPE-UIM2743 v1.3XXXXXX or RXPE-UIM910 v1.3.XXXXXX.
Verify the software version on your device to see if it matches the affected versions listed in the recall.
Reach out to Radiometer America Inc for guidance on next steps if your device is affected.
The affected software versions are RXPE-UIM2743 v1.3XXXXXX or RXPE-UIM910 v1.3.XXXXXX.
Check for the model number ABL90 FLEX Analyzer with reference number REF 393090 and unique device identifier UDI:05700693930909.
Contact Radiometer America Inc for guidance on next steps.
We’ve drafted a message you can send Radiometer to request your refund or repair — edit it as you like.
Subject: Recall Z-2320-2019 — Radiometer Radiometer Hello, I own a Radiometer that is covered by recall Z-2320-2019 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.
