See Luer Cap Set recalled over mold contamination

Recall date

February 17, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Molded Products Inc recalls See Luer Cap Set, MPC-130, set, administration, intravascular

Recall number

Z-1774-2026

FDA classification

Class II

Brand / firm

Molded Products Inc

Sold / distributed

US Nationwide distribution in the states of TN, TX, NV, IL, FL.

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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