Bunnell recalls
Bunnell has 2 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 14 Dec 2022. 1 is still ongoing. The most frequent reason is lead & heavy metals.
Total recalls2since 2012
Last 12 months0reported
Class I150% of total
Ongoing1latest 14 Dec 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 50%Class II 1 50%Class III 0 0%
Why bunnell is recalled
Product types
By year
Ongoing bunnell recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | LifePort Endotracheal Tube Adapters recalled by Bunnell | Bunnell | Lead & Heavy Metals | Nationwide |
All bunnell recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | LifePort Endotracheal Tube Adapters recalled by Bunnell | Bunnell | Lead & Heavy Metals | Nationwide |
| Device | CLASS I | Patient Circuit used with the Life Pulse High Frequency Ventilator recalled | Bunnell | Packaging Defects | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.