Drug recall
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV…
FDA recall event 96696 · Class II · Becton Dickinson Infusion Therapy Systems, Inc.
Key facts
| Event ID | 96696 |
|---|---|
| Recall numbers | Z-1808-2025 |
| Recalling firm | Becton Dickinson Infusion Therapy Systems, Inc. |
| Product type | Devices |
| Products | BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter 20GX1.00IN STRAIGHT BC, REF: 386803; BD Cathena Safety IV Catheter BD Multiguard… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to a manufacturing defect IV catheter may have a hole in the septum, which may result in blood leakage from the septum during insertion, which may cause blood exposure or the need for a second IV… |
| Initiation date | Apr 21, 2025 |
| Report date | May 28, 2025 |
| City | Sandy |
| State | UT |
| Country | United States |
| FEI number | 1710034 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: