Device recall
Z-2458-2024: BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF…
FDA device recall · Class II · Becton Dickinson Infusion Therapy Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2458-2024 |
|---|---|
| Recall event | 94896 |
| Product | BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte Autoguard BC Shielded IV Catheter is intended to be inserted into a patient's peripheral vascular system for short term use to sample blood, monitor… |
| Product code | FOZ |
| Recalling firm | Becton Dickinson Infusion Therapy Systems, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K201075 |
| FEI number | 1710034 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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