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Recall Observatory FDA recall evidence

Device product

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

Z-1679-2017

January 20, 2015

Class II

Product summary

Firm
Molded Products Inc
Event
Event 76760
Status
Terminated
Classification
Class II
Quantity
400 pieces
Official record key
device-enforcement:Z-1679-2017

Official wording

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

Code information: 40013

Distribution pattern: Product was distributed to Ontario, Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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