Device recall
Z-1145-06: Disetronic Ultraflex 8/110 infusion set; (Distributed outside of the US only).
FDA device recall · Class I · Disetronic Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1145-06 |
|---|---|
| Recall event | 34905 |
| Product | Disetronic Ultraflex 8/110 infusion set; (Distributed outside of the US only). |
| Product code | LZG |
| Recalling firm | Disetronic Medical Systems, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 6, 2007 |
| FEI number | 1000116163 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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