# FDA recall Z-2354-2019

> **Molded Products Inc** · Class II · device recall initiated 2019-06-10.

## 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.

## Distribution

Distribution US nationwide.

## Key facts

- **Recall number:** Z-2354-2019
- **Recalling firm:** Molded Products Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-10
- **Report date:** 2019-08-28
- **Termination date:** 2021-05-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Harlan, IA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2354-2019

## Citation

> AI Analytics. FDA recall Z-2354-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2354-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*