Recall
Roche MagNA Pure LC Workstation; Product Numbers: 12236931001, 12236931444, 12236931692 and 03670325001. Robotic workstation for automated isolation of nucleic acids from different kinds of crude sample material such as whole blood,…
Roche Diagnostics Corp. · 9 Feb 2009
- Status
- Recall terminated
- Why, in the FDA's words
- “Protruding screw threads may cut the user when cleaning the interior of the instrument.”
- Recall began
- 9 Feb 2009
- Company
- Roche Diagnostics Corp.
- Device type
- Product code (LXG)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.
