Device recall
Z-0638-2012: Octopus 900 Perimeter, EyeSuite Perimetry version i4.000 (Flash v. 2.1.4 &…
FDA device recall · Class II · Haag-Streit USA Inc
Key facts
| Recall number (Z-number) | Z-0638-2012 |
|---|---|
| Recall event | 60631 |
| Product | Octopus 900 Perimeter, EyeSuite Perimetry version i4.000 (Flash v. 2.1.4 & 2.1.5), Model Number: Octopus 900, Distributed by: Haag-Streit USA, Inc., 3535 Kings Mills Rd., Mason, OH 45040 Product Usage: The OCTOPUS 900 Perimeter is designed for the examination, analysis and documentation of the field… |
| Product code | HJB |
| Recalling firm | Haag-Streit USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2014 |
| 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