FDA Enforcement Class I Ongoing

Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.

Recall: Z-1725-2025 · Reported May 21, 2025

Enforcement

Recall Number
Z-1725-2025
Event ID
96611
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
Baxter Healthcare Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 21, 2025
Initiation Date
April 7, 2025
Classification Date
May 9, 2025
Address
1 Baxter Pkwy, Deerfield, IL, 60015-4625, United States

Description

Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.

Reason

A cybersecurity vulnerability was discovered through internal testing.

Code Info

ALL SERIAL NUMBERS: 1) BT-20-0002, UDI/DI 00815410020537 or 00887761978089; 2) BT-20-0002A, UDI/DI 00815410020537 of 00887761978089; 3) BT-20-0002AP, UDI/DI 00815410020537 or 00887761978089; 4) BT200007, UDI/DI 00815410020278 or 00887761978089; 5) BT-20-0007, UDI/DI 00815410020278 or 00887761978089; 6) BT200011, UDI/DI 00815410020537 or 00887761978089; 7) BT-20-0011, UDI/DI 00815410020537 or 00887761978089; 8) RMS010118CP, UDI/DI 00815410020537 or 00887761978089.

Distribution

Worldwide distribution.

Quantity

4881 units