Guidant Zoom Latitude Programming System, Model 3120, Programmer/Recorder/Monitor (PRM). A portable cardiac rhythm manag
FDA device recall Z-0002-2007 · posted 2006-10-12 · Terminated
Recall details
- Recalling firm
- Guidant Corporation
- Reason for recall
- Final software load did not occur prior to shipment of select programmers.
- Action taken
- Sales Representatives were asked to retrieve/return identified monitors.
- Root cause
- Other
- Status
- Terminated
- Product code
- LWS
- Quantity affected
- 8
- Distribution
- Nationwide distribution --- including states of AR, MI, PA
- Date initiated
- 2006-05-19
- Date posted
- 2006-10-12
- Date terminated
- 2006-12-31
- Location
- Saint Paul, MN
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