Class I

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

Baxter Healthcare Corporation · April 7, 2025

Reason for Recall

A cybersecurity vulnerability was discovered through internal testing.

Distribution

Worldwide distribution.

Quantity Affected

4174 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1726-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Baxter Healthcare Corporation Medical Device Recall: Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP. | SafeCheck