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Baxter Healthcare Corporation recalls Infusion Pump
Recalled March 3, 2021 · FDA recall Z-1150-2021 · Baxter Healthcare
Hazard
Battery performance issues related to prolonged storage. · FDA Class II
Units
589,704 total units
Sold at
Domestic Distribution: ST, AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Puerto Rico. International Distribution: Canada, Barbados, Bermuda, St. Thomas, Guyana, Trinidad and Tobago, Jamaica and Nassau Bahamas.
Description
Battery performance issues related to prolonged storage.
Product
Infusion Pump
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →