Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
Reported: January 22, 2025 Initiated: December 20, 2024 #Z-0884-2025
Product Description
Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
Reason for Recall
There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 187 units
- Distribution
- US, Nationwide Distribution
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002. Recalled by Baxter Healthcare Corporation. Units affected: 187 units.
Why was this product recalled? ▼
There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 22, 2025. Severity: Critical. Recall number: Z-0884-2025.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11