Device recall
Z-0002-2007: Guidant Zoom Latitude Programming System, Model 3120…
FDA device recall · Class III · Guidant Corporation
Key facts
| Recall number (Z-number) | Z-0002-2007 |
|---|---|
| Recall event | 35672 |
| Product | Guidant Zoom Latitude Programming System, Model 3120, Programmer/Recorder/Monitor (PRM). A portable cardiac rhythm management system designed to be used with Guidant implantable pulse generators. Guidant Corporation, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. |
| Product code | LWS |
| Recalling firm | Guidant Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 31, 2006 |
| PMA numbers | P910077 |
| FEI number | 2124215 |
At a glance
- None Linked 510(k)s
- 1–9 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