Device recall
Z-1001-2007: Ascensia Contour Blood Glucose Monitoring System ( Bayer)Diabetes Care System…
FDA device recall · Class I · Bayer Healthcare LLC
Key facts
| Recall number (Z-number) | Z-1001-2007 |
|---|---|
| Recall event | 38118 |
| Product | Ascensia Contour Blood Glucose Monitoring System ( Bayer )Diabetes Care System; Product 7152A.---NO USA Units are affected---. |
| Product code | LFR |
| Recalling firm | Bayer Healthcare LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 30, 2007 |
| 510(k) numbers | K062058 |
| FEI number | 1826988 |
At a glance
- 1–9 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