Device recall
Z-0048-06: Liberty Glucose Monitoring System; Recalling Firm/Manufacturer: Abbott Diabetes…
FDA device recall · Class I · Abbott Laboratories Medisense Products
Key facts
| Recall number (Z-number) | Z-0048-06 |
|---|---|
| Recall event | 33301 |
| Product | Liberty Glucose Monitoring System; Recalling Firm/Manufacturer: Abbott Diabetes Care, Inc., 1360 South Loop Road, Alameda, CA 94502 |
| Product code | NBW |
| Recalling firm | Abbott Laboratories Medisense Products |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 17, 2006 |
| FEI number | 3002803444 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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