FDA Recall
Terminated
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
Recall: Z-1679-2017
·
Initiated January 20, 2015
Recall
- Recall Number
- Z-1679-2017
- Event Number
- 76760
- Firm
- Molded Products Inc
- FEI Number
- 1000138417
- Product Code
- KOC
- Status
- Terminated
- Root Cause
- Process control
- Initiated
- January 20, 2015
- Posted
- March 24, 2017
- Terminated
- March 30, 2017
- Address
- 1112 Chatburn Ave, Harlan, IA, 51537-2007
Description
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
Reason
A customer relayed a complaint of a leaking dialysis tubing connector.
Action
On 1/20/2015, the recalling firm requested the firm's customer to return units from the affected lot.
Distribution
Product was distributed to Ontario, Canada.
Quantity
400 pieces