Baxter Healthcare Corporation: Medical Device Recall in 2025 - (Recall #: Z-1726-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

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.

Product Classification:

Class I

Date Initiated: April 7, 2025

Date Posted: May 21, 2025

Recall Number: Z-1726-2025

Event ID: 96611

Reason for Recall:

A cybersecurity vulnerability was discovered through internal testing.

Status: Ongoing

Product Quantity: 4174 units

Code Information:

ALL SERIAL NUMBERS: 1) BT-80-0004, UDI/DI 00887761978041 or 00815410020292 or 00887761978072; 2) BT-80-0004A, UDI/DI 00887761978041 or 00815410020292 or 00887761978072; 3) BT-80-0008, UDI/DI 00887761976283; 4) BT-80-0008A, UDI/DI 00887761976283; 5) RMS010093CP, UDI/DI 00887761978041 or 00815410020537 or 00815410020292.

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated