Device recall
Z-0232-2026: t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology…
FDA device recall · Class II · Tandem Diabetes Care, Inc.
Key facts
| Recall number (Z-number) | Z-0232-2026 |
|---|---|
| Recall event | 97403 |
| Product | t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and User Guide when using… |
| Product code | QFG |
| Recalling firm | Tandem Diabetes Care, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K201214, K203234, K240309, K241078 |
| FEI number | 3007981285 |
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