Device recall
Z-0932-2008: Bayer Contour TS blood glucose test strips packaged in packs of 10, 25, 50 and…
FDA device recall · Class II · Bayer Healthcare LLC
Key facts
| Recall number (Z-number) | Z-0932-2008 |
|---|---|
| Recall event | 46207 |
| Product | Bayer Contour TS blood glucose test strips packaged in packs of 10, 25, 50 and 100 strips; Bayer Healthcare, Mishawaka, IN. U.S. Product codes 1820, 1823, 1825 and 9578; 1835 and 1836 (Korea); 1832, 1833 and 1837 (India); 1823 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