Molded Products Luer Lock Set Recall: Mislabeling Risk

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Recalling firmMolded Products Inc1112 Chatburn Ave, N/A · Harlan, IA 51537-2007

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Molded Products Inc is recalling Luer Lock Set (Catalog # MPC-125) because some packages were mislabeled as a different product (MPC-150). This could cause confusion in medical use, but the recall does not require immediate action.

Why it’s dangerous

The mislabeling means some packages of Luer Lock Set (MPC-125) were incorrectly marked as Molded Products Male to Male Luer Adapters (MPC-150). This could lead to confusion during medical procedures if the wrong product is used, but it does not cause physical harm.

Who’s affected

Healthcare professionals using IV administration sets may be affected if they received the mislabeled packages. Patients using these sets are at minimal risk since the mislabeling doesn't affect safety.

How to tell if you have this one

Check for the lot number 20266 and expiration date 11/20/2022 on the packaging. The product is labeled as 'Luer Lock Set - Catalog # MPC-125' but some packages were mislabeled as MPC-150.

Brand
Molded Products
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the lot number 20266 and expiration date 11/20/2022 on the packaging.

✎ GovInfoNow

Questions people ask

Is this product dangerous if mislabeled?

No, the mislabeling does not cause physical harm but could lead to confusion in medical use.

What should I do if I have this product?

The recall does not require action; check the label for the lot number and expiration date.

How can I tell if I have the affected product?

Look for the lot number 20266 and expiration date 11/20/2022 on the packaging. Affected units were mislabeled as MPC-150.

Take action

Contact Molded Products

We’ve drafted a message you can send Molded Products to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2354-2019 — Molded Products Molded Products

Hello,

I own a Molded Products that is covered by recall Z-2354-2019 from Molded Products.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2354-2019 (June 10, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2354-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Molded Products Inc recalls Luer Lock Set - Catalog # MPC-125, for IV administration sets.

Lower-risk recall