[Recalled] Luer Lock Set - Catalog # MPC-125, for IV administration sets. — Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were fou… | FDA 2019-06-10
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Luer Lock Set - Catalog # MPC-125, for IV administration sets. |
|---|---|
| Brand / manufacturer | Molded Products Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2354-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 10 June 2019 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.
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 Molded Products 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.