Molded Products Inc: Medical Device Recall in 2017 - (Recall #: Z-1679-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 20, 2015

Date Posted: April 5, 2017

Recall Number: Z-1679-2017

Event ID: 76760

Reason for Recall:

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

Status: Terminated

Product Quantity: 400 pieces

Code Information:

40013

Distribution Pattern:

Product was distributed to Ontario, Canada.

Voluntary or Mandated:

Voluntary: Firm initiated