FDA Device recall Z-1679-2017
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer
- FDA Device
- Class II
- terminated
- Published 2017-04-05
On 2017-04-05 the FDA classified a Class II recall of Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer by Molded Products, citing A customer relayed a complaint of a leaking dialysis tubing connector.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1679-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-20 |
| Published | 2017-04-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Molded Products |
| Distribution | n/a |
Product
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.
Identifiers
| code_info | 40013 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1679-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.