[Recalled] Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x.x.255 — Infusion pump PCs with specific software/network cards/IP addresses can have ne… | FDA 2023-01-24
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x.x.255 |
|---|---|
| Brand / manufacturer | CareFusion 303, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1192-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 January 2023 |
| EAN / barcode | 10885403801549 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Infusion pump PCs with specific software/network cards/IP addresses can have network/wireless connection failure. Could cause inability to receive new datasets and inability to transfer retrospective analytics data to connected systems. Users with interfaces to electronic medication record or admin discharge transfer, may be unable to receive/send data; infusions may need to be manually programmed
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 →
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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.