Bunnell recalls

Bunnell appears in 2 official U.S. recall notices indexed by RecallRadar, most recently on 2022-12-14.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025
  FDA Device · Class II · 2022-12-14 · Bunnell
• Patient Circuit used with the Life Pulse High Frequency Ventilator
  FDA Device · Class I · 2012-12-26 · Bunnell