Drug recall
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube…
FDA recall event 91103 · Class II · Bunnell, Inc.
Key facts
| Event ID | 91103 |
|---|---|
| Recall numbers | Z-0371-2023 |
| Recalling firm | Bunnell, Inc. |
| Product type | Devices |
| Products | 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside Patient Circuit Kits, Catalog: 938 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Nov 2, 2022 |
| Report date | Dec 14, 2022 |
| City | Salt Lake City |
| State | UT |
| Country | United States |
| FEI number | 1719232 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: