Device recall
Z-2411-2012: Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device…
FDA device recall · Class II · Haag-Streit USA Inc
Key facts
| Recall number (Z-number) | Z-2411-2012 |
|---|---|
| Recall event | 63011 |
| Product | Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the peripheral visual field of a patient. The device projects light on various points of a curved surface, and the patient indicates whether he or she sees the light. |
| Product code | HPT |
| Recalling firm | Haag-Streit USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 29, 2015 |
| FEI number | 1000136533 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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