NIPRO Safe Touch Safety Scalp Vein Set — Class II medical device recall Z-1834-2014
Terminated recall by Nipro Medical Corporation, reported 2014-06-25. There is a possibility of a crack in the CP luer connector. The position of the crack is at the connection sit
| Recall number | Z-1834-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nipro Medical Corporation, Miami, FL, United States |
| Recall initiated | 2013-05-04 |
| Classified | 2014-06-19 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2015-03-02 |
| Countries outside the US | BO, BZ, CA, CL, HN, JM, PY, UY, VE |
| Quantity | 176,000 units |
| Reason classes | packaging |
| Lot numbers | 12H27H, 12H31H, 12I12H, 12I14H, 12I24, 12J11, PR-23G19 |
Product
NIPRO Safe Touch Safety Scalp Vein Set
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 of fluids.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1834-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.