FDA DevicesClass II
See Luer Cap Set, MPC-130, set, administration, intravascular
Published: April 15, 2026Recall ID: Z-1774-2026Category: devicesCountry: US
Reason for Recall / Hazard
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.
Product Description & Identification
See Luer Cap Set, MPC-130, set, administration, intravascular
Additional Source Details
| Field | Value |
|---|---|
| City | Harlan |
| State | IA |
| Event id | 98469 |
| Address 1 | 1812 Industrial Pkwy |
| Code info | UDI +B144MPC1300/$$529105203895, Lot Number 20389 |
| Postal code | 51537-2401 |
| Report date | 20260415 |
| Product type | Devices |
| Product quantity | 26900 units |
| Reason for recall | 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. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260217 |
| Initial firm notification | Letter |
| Center classification date | 20260406 |
Overview
- Recalling FirmMolded Products Inc
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the states of TN, TX, NV, IL, FL.