[Recalled] Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system — Due to affected devices that may have bent female IUI connector and may not be… | FDA 2024-08-15
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system |
|---|---|
| Brand / manufacturer | CareFusion 303, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-3140-2024 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 August 2024 |
| EAN / barcode | 10885403830020 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from CareFusion 303, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.