# FDA recall Z-2741-2020

> **CareFusion 303, Inc.** · Class I · device recall initiated 2020-06-30.

## Product

Alaris System PC Unit Model 8015.  modular infusion pump and monitoring system

## Reason for recall

If one or more screws or washers are loose or missing causing the battery not to be properly secured to the PC Unit, that is running on battery power, the system may experience a power loss with a prolonged, non-silenceable alarm. Power loss may result in an interruption of patient therapy or monitoring.

## Distribution

U.S.: CO, FL, SC, NY, CA, NC, TX, IL, PA, AZ, LA, IN, MA, MO, AR,  WI, HI, OR, OH, KS, MN, MI, WA, UT, MD, TN, CO, NJ, NE, ND, WV, KY, IA, MS, AL, DE, AK, VA, OK, NM, GA, CT, SD, NV, ID, MT, ME, VT, WY, NH, MP, DC, GU, PR, AS, RI.    O.U.S.: TR, QA, CA, AE, KW, MX, IL, SA, CH, NL, BE, TW, ZA, PH, CN, AU, IN, FR, MY, NZ, GB, KR, PK, DE, SG, JP, CU, BH

## Key facts

- **Recall number:** Z-2741-2020
- **Recalling firm:** CareFusion 303, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-30
- **Report date:** 2020-08-12
- **Termination date:** 2024-04-22

- **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-2741-2020

## Citation

> AI Analytics. FDA recall Z-2741-2020. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2741-2020. Source: US FDA. Licensed CC0.

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