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Baxter Healthcare Corporation Recall 86788

Description: Infusion Pump

Baxter Healthcare Corporation Recall 86788 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-1150-2021
Event ID86788
Event DescriptionInfusion Pump
Product TypeDevices
DistributionDomestic 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.
Quantity589,704 total units
Recall ReasonBattery performance issues related to prolonged storage.
Device Classification20210303
Device Code InfoInfusion 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
Center Classification Date20210225
Recall Initiation Date20210106
Recalling FirmBaxter Healthcare Corporation
Initial Notification Letter
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