Drug recall
Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing…
FDA recall event 76760 · Class II · Molded Products Inc
Key facts
| Event ID | 76760 |
|---|---|
| Recall numbers | Z-1679-2017 |
| Recalling firm | Molded Products Inc |
| Product type | Devices |
| Products | Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis blood tubing to the hemodialyzer. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A customer relayed a complaint of a leaking dialysis tubing connector. |
| Initiation date | Jan 20, 2015 |
| Report date | Apr 5, 2017 |
| Termination date | Mar 30, 2017 |
| City | Harlan |
| State | IA |
| Country | United States |
| FEI number | 1000138417 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: