Elcam Minimal Residual Volume Luer-activated Swabable-stockcock — Class II medical device recall Z-1869-2017
Terminated recall by Elcam Medical, Inc., reported 2017-04-26, distributed nationwide. The stopcock was found to have punctures.
| Recall number | Z-1869-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Elcam Medical, Inc., Hackensack, NJ, United States |
| Recall initiated | 2017-02-02 |
| Classified | 2017-04-19 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2018-06-08 |
| Distributed | Nationwide (US) |
| Quantity | 810 |
| Lot numbers | 1670350901 |
Product
Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w gxl:w1/r rbls Product Usage: indicated for fluid flow directional control and for providing access ports for administration of intravenous solutions. Typical uses include pressure monitoring, intravenous fluid administration and transfusion.
Reason for recall
The stopcock was found to have punctures.
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-1869-2017. 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.