Device recall
Z-0485-2012: Raymond Laser alignment guide - Model #1096597/002 Red Laser. Intended to assist…
FDA device recall · Class II · The Raymond Corporation
Key facts
| Recall number (Z-number) | Z-0485-2012 |
|---|---|
| Recall event | 60528 |
| Product | Raymond Laser alignment guide - Model #1096597/002 Red Laser. Intended to assist operators in performing material handling activities such as storing and retrieving pallets and material in and on racking projecting a line onto a pallet or other material storage medium for assisting the operator in… |
| Product code | RER |
| Recalling firm | The Raymond Corporation |
| Recall class | Class II |
| Status | Terminated |
| FEI number | 1000255174 |
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