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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