Molded Products Inc recalls MPC-130 See L:uer Cap Sets due to threaded sleeve detaching during use. Affected units have specific UDI and lot numbers. Contact for replacement.
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.
Molded Products Inc is recalling their MPC-130 See Luer Cap Set because the threaded sleeve can become unattached during medical use. This could lead to improper connections and potential complications for patients needing intravenous treatments.
The threaded sleeve in the MPC-130 See Luer Cap Set can become unattached during use, which may cause improper connections. This could lead to incorrect fluid delivery or contamination risks in medical procedures.
Healthcare professionals using the MPC-130 See Luer Cap Set for intravenous administration are most at risk. Patients receiving IV treatments with this device may experience connection issues.
Check for the model MPC-130 on the product. Affected units have UDI number B144MPC1300 and lot number 20389. This product is sold for intravenous administration.
Verify the model number MPC-130 and UDI number B144MPC1300 on the product label.
Reach out to Molded Products Inc for replacement or repair options.
The threaded sleeve may become unattached during use, which could cause improper connections in medical procedures.
Look for model MPC-130 with UDI number B144MPC1300 and lot number 20389 on the product label.
Contact Molded Products Inc for replacement or repair options.
We’ve drafted a message you can send Molded Products to request your refund or repair — edit it as you like.
Subject: Recall Z-1774-2026 — Molded Products Molded Products Hello, I own a Molded Products that is covered by recall Z-1774-2026 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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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.
