Non-Sterile Double DIN to DIN "Y" Connector — Class II medical device recall Z-1679-2017
Terminated recall by Molded Products Inc, reported 2017-04-05. A customer relayed a complaint of a leaking dialysis tubing connector.
| Recall number | Z-1679-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Molded Products Inc, Harlan, IA, United States |
| Recall initiated | 2015-01-20 |
| Classified | 2017-03-24 |
| Reported by FDA | 2017-04-05 |
| Terminated | 2017-03-30 |
| Countries outside the US | CA |
| Quantity | 400 units |
| Reason classes | packaging |
Product
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
Reason for recall
A customer relayed a complaint of a leaking dialysis tubing connector.
Machine access
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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.