Device recall
Z-1679-2017: Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for…
FDA device recall · Class II · Molded Products Inc
Key facts
| Recall number (Z-number) | Z-1679-2017 |
|---|---|
| Recall event | 76760 |
| Product | Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer. |
| Product code | KOC |
| Recalling firm | Molded Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2017 |
| 510(k) numbers | K003712 |
| FEI number | 1000138417 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database