Device recall
Z-1197-2007: Atkinson Retrobulbar Anesthesia Needles, 25 gauge 1 1/2". Catalog Number…
FDA device recall · Class III · Alcon Research, Ltd
Key facts
| Recall number (Z-number) | Z-1197-2007 |
|---|---|
| Recall event | 38382 |
| Product | Atkinson Retrobulbar Anesthesia Needles, 25 gauge 1 1/2". Catalog Number 8065420920. The product is sold in boxes that contain 10 needles each. |
| Product code | HMX |
| Recalling firm | Alcon Research, Ltd |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 28, 2007 |
| FEI number | 1610287 |
At a glance
- None 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