CareFusion 303, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2717-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class I

Date Initiated: June 30, 2020

Date Posted: August 12, 2020

Recall Number: Z-2717-2020

Event ID: 85691

Reason for Recall:

Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may lead to interruption of communication or power between PC Unit and modules, which may result in an infusion that stops with a CHANNEL DISCONNECTED message, and an audio/visual alarm on the PC Unit and an interruption of therapy or monitoring.

Status: Terminated

Product Quantity: 824277

Code Information:

During cleaning, updated cleaning instructions and IUI covers must be used for all serial numbers. US and OUS serial numbers:

Distribution Pattern:

Worldwide distribution. US nationwide including Guam, Puerto Rico, American Samoa, and Military Pacific. Countries of: TR, QA, CA, AE, KW, MX, GI, IL, SA, CH, NL, BE, TW, ZA, PH, CN, AU, IN, FR, MY, NZ, GB, KR, PK, DE, SG, JP, CU, IT, and BH

Voluntary or Mandated:

Voluntary: Firm initiated