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.
Recall summary
| Recall notices | 2 |
|---|---|
| Published | 2012-12-26 to 2022-12-14 |
| By agency | FDA Device (2) |
| By classification | Class I (1), Class II (1) |
| By status | ongoing (1), terminated (1) |
| Distribution named in notices | US |
Recalls
- 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025
FDA Device · Class II · 2022-12-14 · Bunnell
Reason: Some adaptors, for use with high frequency ventilators, were packaged improperly, and may deform at the tip, which may impair the ability to pass a suction catheter or may affect normal ventilator performance, which may… - Patient Circuit used with the Life Pulse High Frequency Ventilator
FDA Device · Class I · 2012-12-26 · Bunnell
Reason: Customer complaints received indicate the heater wire insulation can melt, causing a short which creates sparking and smoke, in the circuit close to the humidifier cartridge. Bunnell is recalling all lots of circuits di…