Device recall
Z-2414-2023: FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre…
FDA device recall · Class II · Abbott Diabetes Care, Inc.
Key facts
| Recall number (Z-number) | Z-2414-2023 |
|---|---|
| Recall event | 92708 |
| Product | FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System |
| Product code | QLG |
| Recalling firm | Abbott Diabetes Care, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K193371 |
| 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