Class II — Molded Products Inc
| Recalling firm | MOLDED PRODUCTS INC. |
|---|---|
| Registered facility | MOLDED PRODUCTS INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | A customer relayed a complaint of a leaking dialysis tubing connector. |
| Product | Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer. |
| Quantity | 400 pieces |
| Distribution | Product was distributed to Ontario, Canada. |
| Initiated | 2015-01-20 |
| Classified | 2017-03-24 |
| Terminated | 2017-03-30 |
| Recall number | Z-1679-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Molded Products Inc (Z-1679-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76760/
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