Alaris System PC Unit Model 8000 modular infusion pump and monitoring… — Class I medical device recall Z-2740-2020
Terminated recall by CareFusion 303, Inc., reported 2020-08-12, distributed in AK, AL, AR, AS, AZ, CA, CO, CT…. If one or more screws or washers are loose or missing causing the battery not to be properly secured to the PC
| Recall number | Z-2740-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2020-06-30 |
| Classified | 2020-08-06 |
| Reported by FDA | 2020-08-12 |
| Terminated | 2024-04-22 |
| Distributed | 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, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
| Quantity | 37,141 |
| Model numbers | 8000 |
Product
Alaris System PC Unit Model 8000 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2740-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.