[Recalled] AVEA Standard ventilator, 17311-xx (xx = 0 - 14) A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. — Car
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | AVEA Standard ventilator, 17311-xx (xx = 0 - 14) A continuous ventilator intended to mechanically control or assist broad spectrum patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. |
|---|---|
| Brand / manufacturer | Carefusion 211 Inc dba Carefusion |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1889-2016 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 17 May 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).
This Class I 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
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Carefusion 211 Inc dba Carefusion
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.