FDA recall, , Moderate risk
Molded Products Luer Cap Sets
The See Luer Cap Set has a threaded sleeve that may not be engaged and can become unattached.
Summary by Recall Canary from the FDA notice
What happened
Molded Products, Inc., of Harlan, Iowa, is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set, a set for administration and intravascular use, based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached. The recall was added to the FDA's Enforcement Report on April 6, 2026, and the company began the recall on February 17, 2026.
The product was distributed nationwide in the states of Tennessee, Texas, Nevada, Illinois, and Florida. The recall was classified by the FDA on April 6, 2026, and in the FDA's weekly enforcement report on April 15, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your set affected?
Match the UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
See Luer Cap Set, MPC-130, set, administration, intravascular
- UDI-DI
- 529105203895
- Lot code
- 20389
Recall details
- Company began the recall
- Company
- Molded Products IncHarlan, Iowa
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98469
- Recall number
- Z-1774-2026
- Quantity recalled
- 26900 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
