FDA recall Z-1726-2025

Baxter Healthcare Corporation · Class I · device

Product

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.

Distribution

Worldwide distribution.

Key facts

Status
Ongoing
Initiation date
2025-04-07
Report date
2025-05-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1726-2025