Device recall
Z-1023-2026: FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The…
FDA device recall · Class I · Abbott Diabetes Care, Inc.
Key facts
| Recall number (Z-number) | Z-1023-2026 |
|---|---|
| Recall event | 98049 |
| Product | FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. |
| Product code | QLG |
| Recalling firm | Abbott Diabetes Care, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K212132 |
| FEI number | 3002803444 |
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