[Recalled] NIPRO Safe Touch Safety Scalp Vein Set — There is a possibility of a crack in the CP luer connector | FDA 2013-05-04
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | NIPRO Safe Touch Safety Scalp Vein Set |
|---|---|
| Brand / manufacturer | Nipro Medical Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1834-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 May 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: There is a possibility of a crack in the CP luer connector. The position of the crack is at the connection site of the CP luer connector and the tubing. The crack could cause or contribute to leakage of fluids.
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 Nipro Medical 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.