Mar Cor Purification CWP Reverse Osmosis System — Class II medical device recall Z-1201-2014
Terminated recall by Mar Cor Purification, reported 2014-03-19, distributed nationwide. There exists a potential situation with the crimp connection at the pump head assembly. The potential exists t
| Recall number | Z-1201-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mar Cor Purification, Minneapolis, MN, United States |
| Recall initiated | 2012-06-27 |
| Classified | 2014-03-13 |
| Reported by FDA | 2014-03-19 |
| Terminated | 2014-08-22 |
| Distributed | Nationwide (US) |
| Quantity | 130 |
| Serial numbers | 1289064, 1289069, 1289159, 1289259, 1289387, 1289650, 1289747, 1289826, 1289949, 1290088, 1290151, 1290333, 1290367, 1290480, 1290489, 1290845, 1290988, 1291042, 1291120, 1291233, 1291373, 1291378, 1291634, 1291777, 1291828 and 104 more |
| Model numbers | 101, 102, 104, 106 |
Product
Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106.
Reason for recall
There exists a potential situation with the crimp connection at the pump head assembly. The potential exists that the reverse osmosis pump head wiring could build resistance resulting in resistive heating of the surrounding components. If this occurs, the pump head assembly may experience melting of the plastic components and potentially create smoke/fire and shut down of the unit.
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-1201-2014. 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.