# FDA recall Z-2939-2020

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

## Product

BD Alaris System PC Unit Model 8100 (Pump Module) and Pump Module Door Assembly Replacement Kits (P/N 49000239, 49000346, 49000438, 49000439) infusion pump.

## Reason for recall

Pump Module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress potentially resulting in a delay to the start of infusion or interruption of infusion. Delays in an infusion or interruption can cause serious injury or death in high-risk patient populations.

## Distribution

Worldwide:  US* (AK, AL, AR, 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, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY);  United Arab Emirates (AE);  Australia (AU);  Canada (CA);  Hungary (HU);  Israel (IL);  Japan (JP)*  Kuwait (KW);  New Zealand (NZ);  Philippines (PH);  Qatar (QA);  Saudi Arabia (SA);  Singapore (SG);  Taiwan (TW);  Turkey (TR)*.    *There are 159 U.S. government and/or military consignees including two located in Japan (JP) and Turkey (TR).

## Key facts

- **Recall number:** Z-2939-2020
- **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-2939-2020

## Citation

> AI Analytics. FDA recall Z-2939-2020. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-2939-2020. Source: US FDA. Licensed CC0.

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