Baxter Healthcare recalls Welch Allyn Life2000 Compressors with specific product codes due to a cybersecurity vulnerability found during internal testing.
A cybersecurity vulnerability was discovered through internal testing.
Baxter Healthcare is recalling Welch Allyn Life2000 Compressors with certain product codes because of a cybersecurity vulnerability discovered through internal testing. This recall affects medical devices used in healthcare settings where security could be compromised.
A cybersecurity vulnerability was discovered through internal testing. This means the device could be susceptible to unauthorized access or data breaches, potentially compromising patient information and device functionality.
Healthcare providers and medical facilities that use Welch Allyn Life2000 Compressors with the listed product codes are most at risk. Patients using these devices may face potential security risks if the vulnerability is exploited.
Check the product code on the device, which includes codes like BT-80-0004, BT-80-0004A, BT-80-0008, BT-80-0008A, or RMS010093CP. Also, verify the serial numbers listed in the recall notice for specific UDI/DI codes.
Identify the product code on your device, which may be BT-80-0004, BT-80-0004A, BT-80-0008, BT-80-0008A, or RMS010093CP.
The recall is due to a cybersecurity vulnerability discovered through internal testing.
Product codes include BT-80-0004, BT-80-0004A, BT-80-0008, BT-80-0008A, and RMS010093CP.
The recall does not specify a stop-use instruction; the remedy is null, so users may continue using the device but should check for security updates.
We’ve drafted a message you can send Welch Allyn to request your refund or repair — edit it as you like.
Subject: Recall Z-1726-2025 — Welch Allyn Welch Allyn Hello, I own a Welch Allyn that is covered by recall Z-1726-2025 from Welch Allyn. 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.
