# FDA recall Z-2651-2020

> **Carefusion 2200 Inc** · Class II · device recall initiated 2020-05-28.

## Product

Safe-T-Centesis 8 Fr Catheter Drainage Tray

## Reason for recall

The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.

## Distribution

370 US customers and 13 distributors.  Product distributed in: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MD, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY    Customer listed, including Federal distribution, uploaded.

## Key facts

- **Recall number:** Z-2651-2020
- **Recalling firm:** Carefusion 2200 Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-28
- **Report date:** 2020-07-29
- **Termination date:** 2024-09-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Vernon Hills, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2651-2020

## Citation

> AI Analytics. FDA recall Z-2651-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2651-2020. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
