Synchron LX Systems Primary Tube Sample Template (a piece of ''labeling'' for use with the Synchron LX 20 and LX 20 Pro
FDA device recall Z-1077-03 · posted 2003-08-06 · Terminated
Recall details
- Recalling firm
- Beckman Coulter Inc
- Reason for recall
- Dead volume on sight gauge for the Synchron LX 20 and LX 20 Pro Systems not stated, which may result in instrument error.
- Action taken
- A revised template with a recall letter was sent to customers with a response request on 19 June 2003.
- Root cause
- Other
- Status
- Terminated
- Quantity affected
- 502
- Distribution
- USA and Canada.
- Date initiated
- 2003-06-19
- Date posted
- 2003-08-06
- Date terminated
- 2004-12-01
- Location
- Brea, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.