# FDA recall Z-0504-2026

> **Becton Dickinson & Company** · Class II · device recall initiated 2025-10-14.

## Product

BD Luer Tip Caps;  Catalog Number(s) or Model Number(s): 308341;

## Reason for recall

BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.

## Distribution

Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Canada, Singapore, Hong Kong.

## Key facts

- **Recall number:** Z-0504-2026
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-14
- **Report date:** 2025-11-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0504-2026

## Citation

> AI Analytics. FDA recall Z-0504-2026. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-0504-2026. Source: US FDA. Licensed CC0.

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