Mar Cor Purification Millenium HX Portable Reverse Osmosis System — Class II medical device recall Z-1213-2014
Terminated recall by Mar Cor Purification, reported 2014-03-26, distributed nationwide. High inlet water pressure beyond specification and the solenoid valve does not meet application which could re
| Recall number | Z-1213-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mar Cor Purification, Minneapolis, MN, United States |
| Recall initiated | 2013-06-26 |
| Classified | 2014-03-14 |
| Reported by FDA | 2014-03-26 |
| Terminated | 2015-01-22 |
| Distributed | Nationwide (US) |
| Quantity | 232 units |
| Serial numbers | 1294627, 1298383, 1298386, 1299352, 1299353, 1299354, 1299355, 1299356, 1299486, 1299487, 1299488, 1299489, 1299503, 1299572, 1299712, 1299713, 1299716, 1299718, 1299719, 1299720, 1299740, 1299742, 1299777, 1299779, 1299780 and 207 more |
| Model numbers | 3025975 |
Product
Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model 3025975. Product Usage: Water Purification System is intended to be used as a dialysis accessory to produce water through reverse osmosis for use with hemodialysis equipment..
Reason for recall
High inlet water pressure beyond specification and the solenoid valve does not meet application which could result in a delay in treatment.
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-1213-2014. 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.