Device recall
Z-0931-2008: Bayer Contour TS blood glucose monitoring system with 10 blood glucose test…
FDA device recall · Class II · Bayer Healthcare LLC
Key facts
| Recall number (Z-number) | Z-0931-2008 |
|---|---|
| Recall event | 46207 |
| Product | Bayer Contour TS blood glucose monitoring system with 10 blood glucose test strips enclosed; Bayer Healthcare, Mishawaka, IN. Products 1802 and 1802N (U.S.), 1810 (Korea), 1811 (India, Korea and Mexico) and 1825 (Mexico). |
| Product code | LFR |
| Recalling firm | Bayer Healthcare LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 7, 2009 |
| FEI number | 1826988 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database