Device recall
Z-1048-2012: "***REF NL82059-01***INTEGRA NEUROSCIENCES***Touhy Needle***Non Sterile for…
FDA device recall · Class II · Integra Neurosciences PR, Inc.
Key facts
| Recall number (Z-number) | Z-1048-2012 |
|---|---|
| Recall event | 60599 |
| Product | "***REF NL82059-01***INTEGRA NEUROSCIENCES***Touhy Needle***Non Sterile for Single Use Only***14 g, 3.5"***Plainsboro, NJ***" Needle for lumbar peritoneal shunt |
| Product code | JXG |
| Recalling firm | Integra Neurosciences PR, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2013 |
| 510(k) numbers | K811288 |
| FEI number | 3000204775 |
At a glance
- 1–9 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