Harlan, IA, United States
Molded Products Inc recalls
2 recalls recorded since 2018, most recently on 17 February 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 17 February 2026
- 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.
- Distribution
- US Nationwide distribution in the states of TN, TX, NV, IL, FL.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1774-2026
- See Luer Cap Set, MPC-130, set, administration, intravascular
Terminated Class II Medical devices
- Recall started
- 10 June 2019
- Terminated
- 28 May 2021
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2354-2019
- Luer Lock Set - Catalog # MPC-125, for IV administration sets.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.