Home / Recalls / Medical Devices
Molded Products Inc recalls Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the
Recalled April 5, 2017 · FDA recall Z-1679-2017 · Molded Products
Hazard
A customer relayed a complaint of a leaking dialysis tubing connector. · FDA Class II
Units
400 pieces
Sold at
Product was distributed to Ontario, Canada.
Description
A customer relayed a complaint of a leaking dialysis tubing connector.
Product
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
Manufacturer(s)
Molded Products Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →