# FDA recall Z-2882-2020

> **CareFusion 303, Inc.** · Class I · device recall initiated 2020-08-04.

## Product

BD Alaris System; Alaris Syringe Module Model 8110;   BD Alaris System; Alaris PCA Module Model 8120;   BD Alaris System; Syringe/PCA Sizer Sensor Replacement Kit, P/N 122278652

## Reason for recall

The Alaris PC unit can display incorrect syringe type and/or syringe sizes.  This could result in delays in infusion, under-infusion, or over-infusion.

## Distribution

US - AK, AL, AR, AS, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY  OUS - AE, AU, BE, BH, CA, CH, CN, IN, KW, MX, MY, NL, NZ, PH, QA, SA, TW and ZA

## Key facts

- **Recall number:** Z-2882-2020
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-08-04
- **Report date:** 2020-09-16

- **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-2882-2020

## Citation

> AI Analytics. FDA recall Z-2882-2020. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2882-2020. Source: US FDA. Licensed CC0.

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