Luer Lock Set — Class II medical device recall Z-2354-2019
Terminated recall by Molded Products Inc, reported 2019-08-28, distributed nationwide. Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as
| Recall number | Z-2354-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Molded Products Inc, Harlan, IA, United States |
| Recall initiated | 2019-06-10 |
| Classified | 2019-08-22 |
| Reported by FDA | 2019-08-28 |
| Terminated | 2021-05-28 |
| Distributed | Nationwide (US) |
| Quantity | 130,000 sets |
| Reason classes | labeling |
| Lot numbers | 20266 |
| Model numbers | MPC-125 |
| Expiration dates | 2022-11-20 |
Product
Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2354-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.