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 | Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150. |
| Product | Luer Lock Set - Catalog # MPC-125, for IV administration sets. |
| Quantity | 130,000 sets |
| Distribution | Distribution US nationwide. |
| Initiated | 2019-06-10 |
| Classified | 2019-08-22 |
| Terminated | 2021-05-28 |
| Recall number | Z-2354-2019 |
| 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-2354-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83330/
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