FDA Enforcement
Class II
Ongoing
See Luer Cap Set, MPC-130, set, administration, intravascular
Recall: Z-1774-2026
·
Reported April 15, 2026
Enforcement
- Recall Number
- Z-1774-2026
- Event ID
- 98469
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Molded Products Inc
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- April 15, 2026
- Initiation Date
- February 17, 2026
- Classification Date
- April 6, 2026
- Address
- 1812 Industrial Pkwy, Harlan, IA, 51537-2401, United States
Description
See Luer Cap Set, MPC-130, set, administration, intravascular
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.
Code Info
UDI +B144MPC1300/$$529105203895, Lot Number 20389
Distribution
US Nationwide distribution in the states of TN, TX, NV, IL, FL.
Quantity
26900 units