PlainRecalls
FDA Devices Critical Class I Ongoing

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

Reported: May 21, 2025 Initiated: April 7, 2025 #Z-1726-2025

Product Description

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

Reason for Recall

A cybersecurity vulnerability was discovered through internal testing.

Details

Units Affected
4174 units
Distribution
Worldwide distribution.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.. Recalled by Baxter Healthcare Corporation. Units affected: 4174 units.
Why was this product recalled?
A cybersecurity vulnerability was discovered through internal testing.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 21, 2025. Severity: Critical. Recall number: Z-1726-2025.