Drug recall
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
FDA recall event 97737 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 97737 |
|---|---|
| Recall numbers | Z-0504-2026 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing. |
| Initiation date | Oct 14, 2025 |
| Report date | Nov 26, 2025 |
| City | Franklin Lakes |
| State | NJ |
| Country | United States |
| FEI number | 2243072 |
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: