Bunnell, Inc.
Bunnell, Inc. appears in FDA public data with 2 recalls — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0371-2023, Class II) was initiated on November 2, 2022.
Summary
- Total Recalls
- 2 (1 Class I)
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0371-2023 | Class II | 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal | November 2, 2022 |
| Z-0514-2013 | Class I | Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a requir | November 19, 2012 |