Non-Sterile Double DIN to DIN "Y" Connector recall
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
Why was Non-Sterile Double DIN to DIN "Y" Connector recalled?
A customer relayed a complaint of a leaking dialysis tubing connector.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
40013
- Product
- Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer.
- Recalling firm
- Molded Products Inc
- Quantity
- 400 pieces
- Distribution
- Product was distributed to Ontario, Canada.
- Recall date
- April 5, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)