Z-1679-2017 Class II Terminated
FDA device recall Z-1679-2017 was initiated by Molded Products Inc on January 20, 2015 and is designated Class II. Reason for recall: A customer relayed a complaint of a leaking dialysis tubing connector. The recall status is terminated (terminated March 30, 2017). Affected quantity: 400 pieces.
Recall Details
- Product Type
- Devices
- Report Date
- April 5, 2017
- Initiation Date
- January 20, 2015
- Termination Date
- March 30, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 400 pieces
Product Description
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
Reason for Recall
A customer relayed a complaint of a leaking dialysis tubing connector.
Distribution Pattern
Product was distributed to Ontario, Canada.
Code Information
40013