Medical device recalls Moderate risk

Luer Lock Set - Catalog # MPC-125 recalled over labeling errors

Recall date
June 10, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Molded Products Inc recalls Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Recall number
Z-2354-2019
FDA classification
Class II
Brand / firm
Molded Products Inc
Sold / distributed
Distribution US nationwide.

Why it was recalled

Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.

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

What was recalled

Luer Lock Set - Catalog # MPC-125, for IV administration sets.

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