Baxter Healthcare Corporation: Medical Device Recall in 2021 - (Recall #: Z-1150-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Infusion Pump

Product Classification:

Class II

Date Initiated: January 6, 2021

Date Posted: March 3, 2021

Recall Number: Z-1150-2021

Event ID: 86788

Reason for Recall:

Battery performance issues related to prolonged storage.

Status: Ongoing

Product Quantity: 589,704 total units

Code Information:

Infusion Pump Product codes: 35700ABB, 35700BAX, and 35700BAX2 Battery codes: 35083, 35162, 35195, and 35724. Infusion Pump Product codes: 35700ABB, 35700BAX, 35700BAX2 3570009 Battery codes: 35223 and 36010

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated