Diasorin LIAISON (R) Chemiluminescence Analyzer Model # 15970. Colorimeter, Photometer, Spectrophotometer for clinical u
FDA device recall Z-1042-2009 · posted 2009-03-30 · Terminated
Recall details
- Recalling firm
- Diasorin Inc.
- Reason for recall
- DiaSorin determined that there was a potential for a short to occur in a a residual starter pump electrical cable in the LIAISON (R) Analyzer.
- Action taken
- DiaSorin Inc authorized Field Service Engineer has visited the sites and performed the necessary field correction. Upon completion of their work, the field service engineer generated a Field Service Report and a copy was left with the customer.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- JJQ
- Quantity affected
- 9
- Distribution
- Worldwide Distribution -- USA including states of NC, NJ, PA, CA, WA, MO, UT, and OR and country of Canada.
- Date initiated
- 2008-12-05
- Date posted
- 2009-03-30
- Date terminated
- 2012-05-22
- Location
- Stillwater, MN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| LIAISON 25 OH VITAMIN D (K032844) | DiaSorin, Inc. | 2004-02-12 |