See Luer Cap Set recall (Molded Products Inc)
Medical deviceClass IIOngoing
Summary: Molded Products Inc is recalling 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.
What is being recalled
See Luer Cap Set, MPC-130, set, administration, intravascular
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the states of TN, TX, NV, IL, FL. (states named: Florida, Illinois, Nevada, Tennessee, Texas)
How to tell if yours is affected
UDI +B144MPC1300/$$529105203895, Lot Number 20389
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1774-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | February 17, 2026 |
| Reported | April 15, 2026 |
| Company | Molded Products Inc |
| Company location | Harlan, IA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 26900 units |
More recalls from Molded Products Inc · all medical device recalls · recalls from February 2026