Reported Apr 15, 2026 · Ongoing

See Luer Cap Set, MPC-130, set, administration, intravascular

Molded Products Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Molded Products Inc · 1812 Industrial Pkwy · Harlan, IA · 51537-2401

Is this the product you have?

  • See Luer Cap Set, MPC-130, set, administration, intravascular
Lot codes and dates
    • UDI +B144MPC1300/$$529105203895
    • Lot Number 20389
Amount recalled
26900 units

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.