CareFusion 303, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2909-2020)

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

Product Classification:

Class I

Date Initiated: August 4, 2020

Date Posted: September 16, 2020

Recall Number: Z-2909-2020

Event ID: 85900

Reason for Recall:

The 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, interruption of infusion, or inability to titrate medication. For high-risk patient populations who are receiving life-sustaining infusions, delays in an infusion or interruption can cause serious injury or death.

Status: Ongoing

Product Quantity: 313740

Code Information:

All serial numbers manufactured from April 07, 2017 to Present.

Distribution Pattern:

U.S.:LA, FL, KY, MI, AL, GA, CA, TN, NC, TX, MA, OH, CO, WI, IL, KS, MO, UT, AK, MD, NY, NV, VA, NE, IN, PA, VT, DC, SC, CT, AR, NJ, MT, ND ,HI , NH, WA, DE, ME, OR, MN, AZ, MS, IA, NM, WY, ID, OK, SD, WV, MP, GU O.U.S.: CA, AE, AU, BE, CA, CH, IL, IN, KW, N/A, NL, NZ, PH, QA, SA, SG, TW, US, ZA

Voluntary or Mandated:

Voluntary: Firm initiated