# FDA recall Z-2465-2021

> **CAREFUSION** · Class II · device recall initiated 2021-08-02.

## Product

BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006

## Reason for recall

Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of FL, PA, NC, OH, SC, IL, RI, MO, NY, TN, AL, VA, PR, CA, NE, NJ, MI, MD, NM, LA, KY, NV, ME, OK, WA, MA, WV, TX, AR, OR, KS, GA, VT, IN, WY, AZ, CO, MN, WI, UT, SD, MS, ID, MT, ND, HI, IA, DC, AK, NH, CT, DE, GU and the countries of CA, NZ, TW, AU, BE, VN, AR, MY, TH, KR, ID, PH, SG, BH, SA, HK, IN, CN, BR.

## Key facts

- **Recall number:** Z-2465-2021
- **Recalling firm:** CAREFUSION
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-08-02
- **Report date:** 2021-09-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Diego, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2465-2021

## Citation

> AI Analytics. FDA recall Z-2465-2021. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2465-2021. Source: US FDA. Licensed CC0.

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