[Recalled] L5C4531 X1 Integrated APD Set with Cassette 3-Prong Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide. — Potential presence of leaks from the cassettes, which may be present due to an… | FDA 2018-10-10
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | L5C4531 X1 Integrated APD Set with Cassette 3-Prong Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide. |
|---|---|
| Brand / manufacturer | Baxter Healthcare Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0030-2020 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 10 October 2018 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential presence of leaks from the cassettes, which may be present due to an incomplete seal of the sheeting to the cassette. A leaking cassette could lead to contamination of the sterile fluid path with micro-organisms. This may predispose the patient to peritonitis.
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 Baxter Healthcare Corporation
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.