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 | The recalled product leaks at the connection site. |
| Product | Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing. |
| Quantity | 1200 sets |
| Distribution | Distributed to one customer in Michigan. |
| Initiated | 2012-06-19 |
| Classified | 2013-03-18 |
| Terminated | 2013-08-14 |
| Recall number | Z-0969-2013 |
| 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-0969-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/64471/
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