Reported Mar 3, 2021 · Terminated

Infusion Pump

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 711 Park Ave · Medina, NY · 14103-1036

Is this the product you have?

  • Infusion Pump
Lot codes and dates
  • Infusion Pump Product codes
    • 35700ABB
    • 35700BAX
  • and 35700BAX2 Battery codes
    • 35083
    • 35162
    • 35195
    • and 35724
  • Infusion Pump Product codes
    • 35700ABB
    • 35700BAX
    • 35700BAX2 3570009
  • Battery codes35223 and 36010
Amount recalled
589,704 total units

Where it was sold

Why it was recalled

Battery performance issues related to prolonged storage.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 4, 2026 · Data as of Sep 19, 5:43 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.