Drug recall
NIPRO Safe Touch Safety Scalp Vein Set
FDA recall event 65274 · Class II · Nipro Medical Corporation
Key facts
| Event ID | 65274 |
|---|---|
| Recall numbers | Z-1834-2014 |
| Recalling firm | Nipro Medical Corporation |
| Product type | Devices |
| Products | NIPRO Safe Touch Safety Scalp Vein Set |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | May 4, 2013 |
| Report date | Jun 25, 2014 |
| Termination date | Mar 2, 2015 |
| City | Miami |
| State | FL |
| Country | United States |
| FEI number | 1000132332 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: