Reported Apr 5, 2017 · Terminated

Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the…

Molded Products Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Molded Products Inc · 1112 Chatburn Ave · Harlan, IA · 51537-2007

Is this the product you have?

  • Non-Sterile Double DIN to DIN "Y" Connector
  • Product UsageExtension for connecting hemodialysis blood tubing to the hemodialyzer
Lot codes and dates
  • 40013
Amount recalled
400 pieces

Why it was recalled

A customer relayed a complaint of a leaking dialysis tubing connector.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 30, 2017 · Data as of Sep 19, 4:46 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.