See Luer Cap Set MPC-130
Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
Stop using the See Luer Cap Set MPC-130 immediately. Contact Molded Products Inc. for instructions on return or replacement of the affected product.
Recall at a glance
- Quantity recalled
- 26900 units
Why it was recalled
Molded Products Inc. is recalling the See Luer Cap Set, model MPC-130, an intravascular administration set component, due to reports that the threaded sleeve may not engage properly and become detached during use. The affected product was distributed nationwide in Tennessee, Texas, Nevada, Illinois, and Florida. A detached cap could compromise the integrity of the intravascular line.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
See Luer Cap Set, MPC-130, set, administration, intravascular
- UDI-DI
- 529105203895
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Editorial summary by Recall Canary · summary updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification