Device recall
Z-0969-2013: Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use…
FDA device recall · Class II · Molded Products Inc
Key facts
| Recall number (Z-number) | Z-0969-2013 |
|---|---|
| Recall event | 64471 |
| Product | Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing. |
| Product code | KOC |
| Recalling firm | Molded Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 14, 2013 |
| 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