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 | Ongoing |
| Reason | Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached. |
| Product | See Luer Cap Set, MPC-130, set, administration, intravascular |
| Quantity | 26900 units |
| Distribution | US Nationwide distribution in the states of TN, TX, NV, IL, FL. |
| Initiated | 2026-02-17 |
| Classified | 2026-04-06 |
| Recall number | Z-1774-2026 |
| 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-1774-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98469/
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