CareFusion 303, Inc. recalls Alaris SpO2 Module Model 8210 and Model 8220 - Product Usage: is intended to provide trained healthcare caregivers a way

Recalled August 26, 2020 · FDA recall Z-2826-2020 · CareFusion 303

Hazard

LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim. · FDA Class II

Units

8558

Sold at

Worldwide distribution - U.S. Nationwide distribution including in the states of CO, FL, SC, NY, CA, NC, TX, IL, PA, AZ, LA, IN, MA, MO, AR, WI, HI, OR, OH, NJ, TN, NE, WA, KS, MI, MD, WV, KY, UT, MN, IA, GA, AL, DE, AK, VA, OK, NM, CT, SD, NV, ID, MT, ME, VT, MS, WY, NH, MP, DC, ND, GU, PR, AS, RI and the 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, BH.

Description

LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.

Product

Alaris SpO2 Module Model 8210 and Model 8220 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.

Manufacturer(s)

CareFusion 303, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →