Drug recall
Luer Lock Set - Catalog # MPC-125, for IV administration sets.
FDA recall event 83330 · Class II · Molded Products Inc
Key facts
| Event ID | 83330 |
|---|---|
| Recall numbers | Z-2354-2019 |
| Recalling firm | Molded Products Inc |
| Product type | Devices |
| Products | Luer Lock Set - Catalog # MPC-125, for IV administration sets. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Jun 10, 2019 |
| Report date | Aug 28, 2019 |
| Termination date | May 28, 2021 |
| City | Harlan |
| State | IA |
| Country | United States |
| FEI number | 1000138417 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: