Roche CoaguChek XS System, CoaguChek XS Plus Care Kit, Roche Diagnostics, Indianapolis, IN; Model Number 05021537001. Co
FDA device recall Z-2004-2009 · posted 2009-09-03 · Terminated
Recall details
- Recalling firm
- Roche Diagnostics Operations, inc.
- Reason for recall
- The recommended cleaning procedures for the meter may cause a malfunction and falsely elevated test result reports.
- Action taken
- Roche Diagnostics Operations, Inc. notified Consignees by letter dated July 22, 2009 informing them of the problem and instructing them to use revised cleaning procedures. For further questions, contact Roche Diagnostics Operations, Inc. at 1-317-521-3194.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- GJS
- Quantity affected
- 1,327 in US
- Distribution
- Worldwide Distribution
- Date initiated
- 2009-07-22
- Date posted
- 2009-09-03
- Date terminated
- 2011-04-27
- Location
- Indianapolis, IN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| COAGUCHEK XS PLUS SYSTEM (K071041) | Roche Diagnostics | 2007-05-11 |